Pesticidal compositions and methods of use thereof

ABSTRACT

A pest-combating composition including sodium lauryl sulfate and one or more of C 6-12  fatty acids, preferably lauric and/or capric and/or caprylic acid, soy methyl ester, and 2-undecanone, and methods of combating pests utilizing same, are disclosed. The compositions can include a carrier oil such as silicon oil, soy methyl ester, or a vegetable oil, and can be in the form of an emulsion. The composition may be constituted as a spray composition, an aerosol, a lotion, a paste, or another compositional form. Pests that may be usefully combated with such composition include flying insects, including flies, mosquitoes, and wasps, ants, including arthropods such as fire ants, ticks, fleas, cockroaches, silver fish, thrips, gnats, aphids, Japanese beetles, and agricultural and horticultural arthropods and insects including beetles (potato and bean), flea beetles, fleahoppers, squash bugs, slugs, leaf hoppers, harlequin bugs, milk weed bugs, spiders, mites, lice, rodents, and deer.

CROSS-REFERENCE TO RELATED APPLICATION

The benefit of priority of U.S. Provisional Patent Application No.61/149,114 filed Feb. 2, 2009 is hereby claimed under the provisions of35 U.S.C. §119. The disclosure of said U.S. Provisional PatentApplication No. 61/149,114 is hereby incorporated herein by reference inits respective entirety.

FIELD OF THE INVENTION

The present invention relates to compositions having utility forcombating pests, including ants, fire ants, mosquitoes, ticks, and otherarthropods and insect species.

DESCRIPTION OF THE RELATED ART

In the field of insecticides and pesticides, as well as insect and pestrepellents, much effort has been given to the development ofcompositions that are “environmentally friendly.” Accordingly, there hasbeen a great interest in compositions that are readily biodegradable orotherwise compatible with human and animal use as formulations havinglittle or no toxicity. A limitation associated with developing thesetypes of pesticides is that they tend to be less effective and shortresidual activity. The pesticides need to be developed with synergisticactivity to make them as effective as the toxic chemicals with residualactivity.

Pest species include mosquitoes, ticks, fleas, flies, chiggers, lice,mites, roaches, and other pests, including insect, arachnid, andcrustacean species that are vectors of human disease-causing agents.Mosquitoes and ticks are of primary interest as disease carriers.Mosquitoes and ticks, for example, carry Lyme disease, encephalitis, andother diseases. Mosquitoes and ticks transmit the widest variety ofpathogens out of all blood-sucking arthropods. As a result, there is agreat interest in developing pesticidal compositions, as well asrepellent compositions. It can be advantageous to kill insects andarthropods in a particular crop locus, in a residential area, and in thetransport of foods and other sensitive cargo that can be contaminated byarthropods, and to prevent transporting arthropods between geographicregions, before they can get close enough to humans to transmit disease,and also before they can damage crops. It would be particularlyadvantageous to kill flying insects with a composition with “knock-down”power, so that the insect can not only be killed at a distance, butprevented from attacking a person after it is hit with an ultimatelylethal, but fast-acting pesticidal composition. Current fast actingpesticidal composition are generally restricted to specific uses due totheir toxic and environmentally poisonous characteristics. Current toxicpesticides include permethrin and other pyrethroids. It is of primaryimportance to have a pesticide as effective as these toxic materials,but environmentally sensitive and far less toxic to humans and animals.

It is also of importance, though secondary to pesticidal activity, tohave insect repellents that are efficacious for controlling mosquitoesand ticks on animals and human skin, and which is relatively aseffective, as repellents based on N,N-diethyl-m-toluamide (DEET).

Although there has been increasing use of various natural ingredients inpest-combating compositions, such natural ingredients typically areutilized in the form of isolates or purified species, rather than beingchemically processed to other ingredient forms. This self-imposedlimitation on the formulation of so-called “green” products has in manycases limited the chemical efficacy of the compositions for theirintended pest-combating usage.

In consequence, the art continues to seek improvements in naturalproduct formulations for combating insects and other pests.

SUMMARY OF THE INVENTION

The present invention relates to pest-combating compositions, andmethods of killing and/or repelling pests using the compositions. Thecompositions are preferably DEET-free and pyrethroid-free.

In one embodiment, the compositions contain as active ingredients,sodium lauryl sulfate and one or more C₆₋₁₂ fatty acids, preferablylauric and/or capric and/or caprylic acid. In one aspect of thisembodiment, the compositions further include a carrier. Suitablecarriers include silicon oil, soy methyl ester, or vegetable oils suchas canola, corn, cotton, palm, rapeseed, safflower, soybean, andsunflower oils, and mixtures thereof, and, more specifically, soybeanoil or coconut oil. Soy methyl ester can be preferred among thesecarriers. The compositions can be in the form of an oil-in-wateremulsion, a water-in-oil emulsion, a micelle formulation, a solution, asuspension, a dispersion, and the like. In any of these forms, theformulations can include a propellant, so that they can be aerosolized.Such aerosolized compositions can be used in fumigation applications,such as ship/air cargo or food containment areas. The compositions canalso be used as a pesticide treatment prior to transporting items. Inone embodiment, the compositions are converted to aerosol compositionsby adding nitrogen to the formula, and keeping the contents in apressurized container, such as a metal can. Nitrogen is an inertadditive, and not a green-house gas, and can be preferred over otherpropellants, such as low molecular weight hydrocarbons. When present,the nitrogen is present in an amount of up to 10 percent, though istypically in the range of about 0.5% by weight of the composition.

The sodium lauryl sulfate is typically present in an amount ranging fromabout 0.1 to about 10% by weight of the composition, more typically inan amount ranging from 1.0 to about 5% by weight.

In another embodiment, the compositions contain, as active ingredients,a combination of sodium lauryl sulfate and soy methyl ester, without thefatty acids being present.

In either of these embodiments, the compositions can further include2-undecanone. The presence of 2-undecanone or rue oil further enhancesthe insecticidal/pesticidal activity of the compositions by reducingtime to mortality on specific insects, arachnids, and/or arthropods. Inone embodiment, the 2-undecanone is present by virtue of the compositionincluding rue oil (an essential oil extracted from Ruta graveolens ofthe Rutaceae family, also known as garden rue and herbygrass). Thepresence of 2-undecanone or rue oil increases the pest repellency toinsects, arthropods and animals such as rodents and deer

In a third embodiment, the compositions contain, as active ingredients,a combination of sodium lauryl sulfate and 2-undecanone or rue oil. Inthis embodiment, the compositions can further include fatty acids, avegetable oil such as soybean oil or coconut oil, soy methyl ester,and/or silicon oil. The oils can be part of a water-in-oil oroil-in-water emulsion.

In a fourth embodiment, the formulation does not include oil, and istherefore not an emulsion or micelle. For example, an aqueous solutioncan be prepared including between about 0.5% and 10% sodium laurylsulfate, one or more fatty acids such as lauric, capric or caprylic acidin an amount ranging from 0.5% and 20%, a fatty acid salt, such aspotassium oleate, in an amount ranging from 0.25% and 5%, a humectantsuch as glycerin in an amount ranging from 0.5% and 0%, glycerolmonostearate or other fatty acid mono-glycerides in an amount rangingfrom 0.5% and 20%, with the balance being water, all amounts measuredw/w. 2-undecanone can also be added to this formula to increase activityand repellency at 0.1% to 5%. In addition, the enzyme Subtilisin can beadded to enhance insecticidal activity to this formula from 0.1% to 10%,and can also help control allergens, such as those produced by pests.

Also, the compositions can include a fragrance such as menthol, citral,lemongrass oil, and/or cedar oil, to make the scent more acceptable.Menthol can be preferred in the shampoo version for humans and animalsto control lice, ticks and mites as it also relieves the itch that isfrequently associated with pest infestation.

The compositions can be formulated for application to a human or animal,for example, in the form of sprays, lotions, or liquid compositions, andused, for example, as pesticides, and, in some embodiments, as insectrepellents. In insecticidal uses, the compositions can be used inshampoos, and the like, to kill lice, ticks, fleas, and mites, in bothanimals and humans.

Alternatively, the compositions can be applied to an article or aregion/locus. Typical application rates when applied to a region/locusare in the range of about 0.01 oz/square inch.

The compositions can be combined with an insect attractant and/or afeeding stimulant, particularly in bait applications. The insectattractant and/or feeding stimulant are preferably naturally-occurringinsect attractants or feeding stimulants. Representative examples ofinsect attractants include insect pheromones, and, for mosquitoes, humansweat or its components, or carbon dioxide. Representative feedingstimulants include cucurbitacins, corn oil, peanut oil, and the like. Inthese embodiments, the compositions attract the insects, and then killthem.

In one embodiment, the compositions are combined with a thixotropicagent. In this embodiment, mechanical agitation, such as that whichoccurs when the composition is sprayed, liquefies the composition andallows it to be applied in aerosol form. When the mechanical agitationis stopped, the compositions then return to their original state, forexample, a gel, so that they can remain attached to where they areapplied. The use of a thixotropic agent can enable the formulations tobe prepared without using any oil, and enables the active components tostick on plant surfaces, and protect the plants from insect damage.

In some embodiments, the formulations have insect repellent orinsecticidal properties, but are not phytotoxic. Examples of plants thatcan be treated include shrubs, vegetable gardens, grasses, and trees,such as fruit trees. As such, the formulations can be used asinsecticides, and to prevent insect damage on lawns and in agriculturaland horticultural applications, as well as residential and commercialapplications.

Representative insects that can be killed using the compositionsdescribed herein include ants, cockroaches, beetles (potato and bean),flea beetles, fleahoppers, squash bugs, stink bugs, aphids, thrips,slugs, leaf hoppers, harlequin bugs and milk weed bugs. Representativeinsects that can be repelled using the compositions described hereininclude caterpillars, maggots, moths, and grasshoppers. Rodents and deerwere also repelled with some formulations.

The lack of phytotoxicity, lack of oils, and the use of a thixotropicagent allows the composition to be used primarily as an insecticide andinsect damage preventer for lawns, agricultural and horticulturalapplications, though it is also useful for residential and commercialapplications. The thixotropic agent enables the actives to stick on thesurface of a plant protecting it from insects without the use of an oil.This formula is also able to be certified organic.

Another aspect of the invention relates to a packaged insect repellent,comprising a container holding the pesticidal composition describedherein.

A still further aspect of the invention relates to a method of combatingpests, at a locus containing or susceptible to the presence of same,such method including applying to at least a portion of such locus apesticidal composition as described herein.

In another embodiment, the compositions can be used as a repellent torodents and deer, particularly when the compositions include undecanoneor rue oil, which can find particular application in agricultural andresidential applications.

Other aspects, features and embodiments of the invention will be morefully apparent from the ensuing disclosure and appended claims.

DETAILED DESCRIPTION

The present invention is based on the discovery that sodium laurylsulfate and C₆₋₁₂ fatty acids, preferably lauric, capric and/or caprylicacids, are unexpectedly and highly effective as pest-combating activeingredients in the pest control formulations. The present invention isalso based on the discovery that sodium lauryl sulfate and soy methylester and/or 2-undecanone, with or without C₆₋₁₂ fatty acids such aslauric, capric and/or caprylic acids, are unexpectedly and highlyeffective as pest-combating active ingredients. The compositions of thepresent inventions, and methods of use thereof, are described in detailbelow.

I. Pesticidal Compositions

Main Active Agents

In one embodiment, the pesticidal compositions described herein includesodium lauryl sulfate and one or more C₆₋₁₂ fatty acids, preferablylauric and/or capric and/or caprylic acids.

In another embodiment, the pesticidal compositions described hereininclude sodium lauryl sulfate and/or soy methyl ester (the soy methylester can optionally be replaced or combined with any transesterifiedester) in combination with sodium lauryl sulfate and/or 2-undecanone orrue oil (which includes a significant amount of 2-undecanone).

Combinations of sodium lauryl sulfate and two or more of these activeagents are intended to be within the scope of the invention.

In some embodiments, the compositions further include an enzyme, whichis preferably a protease.

Sodium Lauryl Sulfate

Sodium lauryl sulfate is an emulsifier, an also has insecticidalproperties. Accordingly, when the compositions include sodium laurylsulfate, water, and a carrier oil, such as silicon oil, a vegetable oil,mineral oil, or soy methyl ester, the sodium lauryl sulfate can serve asthe emulsifier. The concentration of sodium lauryl sulfate in thecompositions described herein is typically in the range of about 0.1 toabout 10 percent by weight of the composition, more typically in therange of about 1.0 to about 5 percent by weight of the composition.

Fatty Acids

Fatty Acids give the formulation quick insecticidal activity. The fattyacids are typically in the range of C₆₋₁₂ fatty acids, and, preferably,include lauric and/or capric and/or caprylic acids. One representativefatty acid formulation is C810 (formerly known as LC810 in CIP2 fromPeter Cremer). C810 is supplied by Univar and manufactured by Proctor &Gamble. It is a blend primarily of Capric (octanoic) Acid & Caprylic(Decanoic) Acid.

Undecanone

In some embodiments, the compositions include isolated 2-undecanone orrue oil, the main constituent of which is 2-undecanone. 2-Undecanonealso gives the formulation quick insecticidal activity. In someembodiments, the 2-undecanone functions as an insect repellent, ratherthan an insecticide. For example, compositions containing 2-undecanoneexhibit repellency against mosquitoes, ticks, cockroaches, thrips, deerfly, gnats, aphids, and the like. In other embodiments, the 2-undecanonefunctions or rue oil to enhance the pesticidal effectiveness of thecompositions. The 2-undecanone enhances the pest repellency of thecompositions to repel animals such as rodents and deer.

Due to the volatility of 2-undecanone, it can be desirable to formulatethe composition containing such ingredient with a sticking agent, sothat the 2-undecanone in the composition persists at the point ofapplication, to extend the duration of active repellency of thecomposition.

Soy Methyl Ester

Soy methyl ester (also referred to herein as “SME”) is an optionalactive agent, and can serve a dual role. It can serve not only as anactive agent, enhancing the pesticidal activity and insect repellency ofthe compositions, but also as a base for an emulsion incorporating thecomposition. SME also is a solvent to 2-undecanone, and can providestable emulsions and control the rate of volatile 2-undecanone releaseover time.

As used herein, the term “soy methyl ester” refers to methyl ester(s) offatty acids or oleochemicals of soybean oil, and sometimes is referredto as soybean oil methyl ester or as soybean methyl ester. Soy methylesters are readily produced by subjecting fatty acids and oleochemicalsof soybean oil to transesterification chemical reaction, e.g., abase-catalyzed transesterification of soybean oil. Soy methyl esters ofwidely varying types are usefully employed in the practice of theinvention. One particularly preferred soy methyl ester comprises amixture of C₁₆-C₁₈ saturated and C₁₈ unsaturated methyl esters,identified by Chemical Abstracts Registry Number (CAS#) 67762-38-3.

Soy methyl esters usefully employed in compositions of the presentinvention are readily commercially available, e.g., under the brand name“Enviro-Saver” from Columbus Foods Company (Chicago, Ill.), under thebrand name “Ecoline Soya Methyl Esters” from Cortec Corporation (St.Paul, Minn.), and otherwise as fatty acid methyl ester from CargillIndustrial Oils & Lubricants (Minneapolis, Minn.), as methyl soyate fromCognis Corporation (Cincinnati, Ohio), and as soy methyl esters fromVertec BioSolvents, Inc. (Downers Grove, Ill.), Lambent TechnologiesCorporation (Gurnee, Ill.), soy-based fatty acid esters from ChemolCompany, Inc. (Greensboro, N.C.), SoyGold 1000 from Ag EnvironmentalProducts (Omaha, Nebr.), and Steposol SB-D and Stepasol SB-W soy methylesters from Stepan Company (Northfield, Ill.).

The soy methyl ester can be used at any suitable concentration in thecompositions of the invention. Preferably, the soy methyl ester has aconcentration in the composition of from about 2% to about 15% byweight, based on the total weight of the composition. More preferably,the soy methyl ester has a composition concentration in a range of fromabout 2.4% to about 12% by weight, based on total weight of thecomposition. Most preferably, the soy methyl ester has a concentrationin the composition in a range of from about 3 to about 10% by weight,based on total weight of the composition.

In place of, or in addition to, the soy methyl ester, othertransesterified triglycerides can be used, including methyl and otherC₁₋₁₀ alkyl esters of other triglycerides, and C₂₋₁₀ alkyl esters of thefatty acids found in soybean oil.

Feeding Stimulants/Attractants

The efficacy of the compositions can, in some embodiments, be enhancedby using a feeding stimulant and/or attractant. This is particularlytrue where the compositions are used in bait applications. The use offeeding stimulants and attractants allow one to apply the insecticidalcompositions at a reduced rate over a given locus, such as a crop locus.

Bait stations typically deliver an insecticide through a sealed plasticor metal chamber that insects enter. This gives bait stations theadvantage of decreasing both the amount of insecticide used and thelikelihood of exposure to it. Where, as here, the compositions typicallyinclude essentially harmless components, the main use for bait stationsis to lure the insects away from areas of concern, such as where cropsare growing, children are present, or food is prepared or stored.

Ideally, the feeding stimulants and/or attractants arenaturally-occurring substances.

For termites, one type of feeding stimulant is sitosterol. Sitosterol isknown to increase feeding or induce phagostimulatory responses by alltermite species. Termite species known to show increased feeding oncellulosic baits containing sitosterol include Coptotermes formosanus,Reticulitermes tibialis, Reticulitermes flavipes, and Reticulitermesvirginicus. Sitosterol can also be used in connection with otherimportant pest species of termites, in particular: Reticulitermeshesperus, Reticulitermes hageni, and Heterotermes species.

Representative examples of insect attractants for mosquitoes includehuman sweat or its components, and carbon dioxide.

Representative feeding stimulants for fire ants include corn oil, peanutoil, and the like.

Cucurbitacin-based feeding stimulants can be used to control insects inthe Diabrotica family, including adult western corn rootworms,Diabrotica virgifera virgifera. Representative feeding stimulants forDiabrotica include cucurbitacin

The green mirid, Creontiades dilutus is a true bug (order Hemiptera,suborder Heteroptera), characterized by piercing and sucking mouthparts.The green mirid is a pest of cotton, and is found in other crops, suchas lucerne, potatoes, soy beans, stone fruits, sunflower and grapes. Amixture of hexyl hexanoate and (E)-2-hexenyl hexanoate is an insectpheromone for the green mirid.

Additional feeding stimulants and attractants, where the term attractantis intended to include pheromones and kairomones, include:

Z-5-decenyl acetate, dodecanyl acetate, Z-7-dodecenl acetate,E-7-dodecenyl acetate, Z-8-dodecenyl acetate, E-8-dodecenyl acetate,Z-9-dodecenyl acetate, E-9-dodecenylacetate, E-10-dodecenyl acetate,11-dodecenyl acetate, Z-9,11-dodecadienyl acetate, E-9,11-dodecadienylacetate, Z-11-tridecenyl acetate, E-1-tridecenyl acetate, tetradecenylacetate, E-7-tetradecenyl acetate, Z-8-tetradecenyl acetate,E-8-tetradecenyl acetate, Z-9-tetradecenyl acetate, E-9-tetradecenylacetate, Z-10-tetradecenyl acetate, E-10-tetradecenyl acetate,Z-11-tetradecenyl acetate, E-11-tetradecenyl acetate, Z-12-pentadecenylacetate, E-12-pentadecenyl acetate, hexadecenyl acetate, Z-7-hexadecenylacetate, Z-11-hexadecenyl acetate, E-11-hexadecenyl acetate, octadecanylacetate, E,Z-7,9-dodecadienyl acetate, Z,E-7,9-dodecadienyl acetate,E,E-7,9-dodecadienyl acetate, Z,Z-7,9-dodecadienyl acetate,E,E-8,10-dodecadienyl acetate, E,Z-9,12-dodecadienyl acetate,E,Z-4,7-tridecadienyl acetate, 4-methoxy-cinnamaldehyde, .beta.-ionone,estragole, eugenol, indole, 8-methyl-2-decyl propanoate,E,E-9,11-tetradecadienyl acetate, Z,Z-9,12-tetradecadienyl acetate,Z,Z-7,11-hexadecadienyl acetate, E,Z-7,11-hexadecadienyl acetate,Z,E-7,11-hexadecadienyl acetate, E,E-7,11-hexadecadienyl acetate,Z,E-3,13-octadecadienyl acetate, E,Z-3,13-octadecadienyl acetate,E,E-3,13-octadecadienyl acetate, ethanol, hexanol, heptanol, octanol,decanol, Z-6-nonenol, E-6-nonenol, dodecanol, 11-dodecenol,Z-7-dodecenol, E-7-dodecenol, Z-8-dodecenol, E-8-dodecenol,E-9-dodecenol, Z-9-dodecenol, E-9,11-dodecadienol, Z-9,11-dodecadienol,Z,E-5,7-dodecadienol, E,E-5,7-dodecadienol, E,E-8,10-dodecadienol,E,Z-8,10-dodecadienol, Z,Z-8,10-dodecadienol, Z,E-8,10-dodecadienol,E,Z-7,9-dodecadienol, Z,Z-7,9-dodecadienol, E-5-tetradecenol,Z-8-tetradecenol, Z-9-tetradecenol, E-9-tetradecenol, Z-10-tetradecenol,Z-11-tetradecenol, E-11-tetradecenol, Z-11-hexadecenol,Z,E-9,11-tetradecadienol, Z,E-9,12-tetradecadienol,Z,Z-9,12-tetradecadienol, Z,Z-10,12-tetradecadienol,Z,Z-7,11-hexadecadienol, Z,E-7,11-hexadecadienol,(E)-14-methyl-8-hexadec-en-1-ol, (Z)-14-methyl-8-hexadecen-1-ol,E,E-10,12-hexadecadienol, E,Z-10,12-hexadecadienol, dodecanal,Z-9-dodecenal, tetradecanal, Z-7-tetradecenal, Z-9-tetradecenal,Z-11-tetradecenal, E-11-tetradecenal, E-11,13-tetradecadienal,E,E-8,10-tetradecadienal, Z,E-9,11-tetradecadienal,Z,E-9,12-tetradecadienal, hexadecanal, Z-8-hexadecenal, Z-9-hexadecenal,Z-10-hexadecenal, E-10-hexadecenal, Z-11-hexadecenal, E-11-hexadecenal,Z-12-hexadecenal, Z-13-hexadecenal, (Z)-14-methyl-8-hexadecenal,(E)-14-methyl-8-hexadecenal, Z,Z-7,11-hexadecadienal,Z,E-7,11-hexadecadienal, Z,E-9,11-hexadecadienal-,E,E-10,12-hexadecadienal, E,Z-10,12-hexadecadienal,Z,E-10,12-hexadecadienal, Z,Z-10,12-hexadecadienal,Z,Z-11,13-hexadecadienal, octadecanal, Z-11-octadecenal,E-13-oxtadecenal, Z-13-octadecenal, Z-5-decenyl-3-methyl-butanoateDisparlure: (+) cis-7,8-epoxy-2-methyloctadecane, Seudenol:3-methyl-2-cyclohexen-1-ol, sulcatol: -methyl-5-hepten-2-ol, Ipsenol:2-methyl-6-methylene-7-octen-4-ol, Ipsdienol:2-methyl-6-methylene-2,7-octadien-4-ol, Grandlure I:cis-2-isopropenyl-1-methyl-cyclobutanethanol, Grandlure II:Z-3,3-dimethyl-1-cyclohexanethanol, Grandlure III:Z-3,3-dimethyl-1-cyclohexaneacetaldehyde, Grandlure IV:E-3,3-dimethyl-1-cyclohexaneacetaldehyde, cis-2-verbenol:cis-4,6,6-trimethylbicyclo[3,1,1]hept-3-en-2-ol cucurbitacin,2-methyl-3-buten-2-ol, 4-methyl-3-heptanol, cucurbitacin,2-methyl-3-buten-2-ol, 4-methyl-3-heptanol, alpha-pinene:2,6,6-trimethylbicyclo[3,1,1]hept-2-ene, alpha-caryophyllene:4,11,11-trimethyl-8-methylenebicyclo[7,2,0]undecane, Z-9-tricosene,alpha-multistriatin 2(2-endo,4-endo)-5-ethyl-2,4-dimethyl-6,8-dioxabicyclo[3,2,1]octane,methyleugenol: 1,2-dimethoxy-4-(2-propenyl)phenol, Lineatin:3,3,7-trimethyl-2,9-dioxatricyclo[3,3,1,0]nonane, Chalcogran:2-ethyl-1,6-dioxaspiro[4,4]nonane, Frontalin:1,5-Dimethyl-6,8-dioxabicyclo[3,2,1]octane, endo-Brevicomin:endo-7-ethyl-5-methyl-6,8-dioxabicyclo[3-,2,1]octan, exo-brevicomin:exo-7-ethyl-5-methyl-6,8-dioxabicyclo[3,2,1]octane,(Z)-5-(1-decenyl)dihydro-2-(3H)-furanone, Farnesol3,7-11-trimethyl-2,6,10-dodecatrien-1-ol, Nerolidol3,7-,11-trimethyl-1,6,10-dodecatrien-3-ol, 3-methyl, 6-(1-methylethenyl)-9-decen-1-ol acetate,(Z)-3-methyl-6-(1-methylethenyl)-3,9-decadien-1-ol acetate,(E)-3,9-methyl-6-(1-methylethenyl)-5,8-decadien-1-ol-acetate,3-methylene-7-methyl-octen-1-ol propionate,(Z)-3,7-dimethyl-2,7-octadien-1-ol propionate,(Z)-3,9-dimethyl-6-(1-methylethenyl)-3,9-decadien-1-ol propionate.

Optional Additional Components

For example, the additional ingredients may include fillers,dispersants, water or other solvent medium or media, surfactants,suspension agents, sticking agents, stabilizers, preservatives, dyes,pigments, masking agents, emollients, excipients, post-applicationdetection agents, and additional active ingredients. For example, thecomposition may be formulated with a sunscreen and/or sunblocking agent.

Such additional active ingredients may include, for example, additionalpest-combating ingredients, such as repellents and/or cidal agents. Byway of example, the compositions may be formulated with an insectrepellent ingredient. The repellents/cidal agents are preferably, butneed not be, naturally-occurring.

Thickening Agents/Sticking Agents

Representative sticking agents include, but are not limited to,polyvinyl acetates, polyvinyl alcohols, dextrins, sugars and vegetableoils.

Thickeners can also be used. Examples of suitable thickeners includeorganic polymers, such as partially or fully neutralized polyacrylicacids (Carbopol®, polyethylene glycols (Polyox®), polyvinyl alcohols andnon-ionically or ionically modified celluloses (Tylose®), xanthan-basedthixotropic thickeners (Kelzan®), and also inorganic dispersethickeners, such as precipitated or pyrogenic silicas, kaolins,bentonites and aluminum/silicon mixed oxides. Potassium oleate isanother thixotropic agent, and is present in the formulation describedin Example 4 below. In some embodiments, the formulation includes sodiumlauryl sulfate, fatty acids and thixotropic agents, but does not includean oil.

Naturally-Occurring Repellent/Cidal Agents

In one embodiment, the additional repellent or cidal agents areessential oils or plant extracts.

Plant Extracts

Representative plant extracts (botanical insecticides) include:

Neem, azadirachtin, limonene, capsaicin, pyrethrum and pyrethrins,garlic,

Neem is made from extracts of Neem tree seeds, and is used to control awide variety of insects including leafminers, whiteflies, thrips,caterpillars, aphids, mealybugs, spider mites, scale crawlers, andbeetles. Azadirachtin is the active ingredient in neem extracts. Neemtends to not produce a quick knockdown or kill, but stops insectfeeding.

Limonene (also known as d-Limonene) is produced from citrus oilsextracted from oranges and other citrus fruit peels. It is used as acontact insecticide against ants, roaches, palmetto bugs, fleas,silverfish, fire ants, and many other insects. Limonene is the activeingredient in Ortho Home Defense Indoor Insect Killer, Concern CitrusHome Pest Control, and Citrex Fire Ant Killer.

Capsaicin is the material that makes chili peppers hot, and is used tocontrol (mainly to repel) aphids, spider mites, thrips, whitefly, lacebugs, leafhoppers, and other pests.

Pyrethrum is made from the finely powdered flowers of a species ofdaisy. The word pyrethrum is the name for the crude flower dust itself,and the term pyrethrins refers to the insecticidal compounds that areextracted from pyrethrum. Pyrethroids are not botanical insecticides,but synthetic pesticides that are very similar in structure to thepyrethrins.

Pyrethrum is a contact insecticide and must be applied directly to theinsect to be effective. Pyrethrum rapidly paralyzes pests, but may notkill them. Pyrethrum and pyrethrins are often formulated with anotherinsecticide to ensure that paralyzed insects do not recover.

Essential Oils

There are a number of essential oils or components of essential oilswith insecticidal properties. Examples include the oils of cedar,cinnamon, citronella, citrus, clove, eugenol (a component of clove oil),garlic, mints, such as peppermint and spearmint, rosemary, and severalothers. As insecticides, these work most commonly as contact killingagents only, so re-treatment may be needed. Most essential oils used aspesticides work by disrupting an insect neurotransmitter that is notpresent in people, pets, or other vertebrates.

Peppermint oil, one example of an essential oil with cidal properties,is particularly active against ants, roaches, waterbugs, silverfish,crickets, spiders and centipedes.

Fragrances

The compositions can include one or more fragrances, which, in someembodiments, are essential oils such as those described above. Althoughit can be preferred to use natural components, the fragrances caninclude non-naturally occurring chemicals. In some embodiments, thefragrance can also impart a beneficial property to the compositions, forexample, where menthol is used as both a fragrance and an anti-itchcomponent when the compositions are applied to human or animal skin.

Representative fragrances include floral or plant oil fragrances such ascitrus, clove, eucalyptus, wintergreen, rosemary, citronella or cinnamonoil, which also possesses pesticidal and antimicrobial properties.

A wide variety of chemicals are known for perfumery, such as aldehydes,ketones, esters, alcohols, terpenes, and the like. Most conventionalfragrance materials are volatile essential oils.

Natural fragrances include naturally derived oils such as oil ofBergamot, Bitter Orange, Lemon, Mandarin, Caraway, Cedar Leaf, CloveLeaf, Cedar Wood, Geranium, Lavender, Orange, Origanum, Petitgrain,White Cedar, Patchouli, Lavandin, Neroli, Rose absolute, and the like.Natural perfumes include the extracts of blossoms, stems and leaves,fruits, fruit peel, roots, woods, herbs and grasses, needles andbranches, resins and balsams. Other suitable perfume oils are essentialoils of relatively low volatility which are mostly used as aromacomponents. Examples include sage oil, chamomile oil, clove oil, melissaoil, mint oil, cinnamon leaf oil, lime-blossom oil, juniper berry oil,vetivert oil, olibanum oil, galbanum oil, ladanum oil and lavendin oil.

Typical synthetic perfume compounds are products of the ester, ether,aldehyde, ketone, alcohol and hydrocarbon type. Examples of perfumecompounds of the ester type are benzyl acetate, p-tert-butylcyclohexylacetate, linalyl acetate, phenyl ethyl acetate, linalylbenzoate, benzyl formate, allyl cyclohexyl propionate, styrallylpropionate and benzyl salicylate. Ethers include, for example, benzylethyl ether while aldehydes include, for example, the linear alkanalscontaining 8 to 18 carbon atoms, citral, citronellal,citronellyloxyacetaldehyde, cyclamen aldehyde, hydroxycitronellal,lilial and bourgeonal. Examples of suitable ketones are the ionones andmethyl cedryl ketone. Suitable alcohols are anethol, citronellol,eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol andterpineol. The hydrocarbons mainly include the terpenes and balsams.

Other artificial liquid fragrances include geraniol, geranyl acetate,eugenol, isoeugenol, linalool, linalyl acetate, phenethyl alcohol,methyl ethyl ketone, methylionone, isobornyl acetate, and the like.

Non-Naturally Occurring Repellent or Cidal Agents

While it can be preferred in some embodiments for the compositions to becapable of being organically certified, as including only naturalingredients, in another embodiment, the additional repellent or cidalagents are non-naturally occurring substances. Representative repellentand cidal agents include compounds or compositions that are used asacaricides, insecticides, insecticide synergists, ixodicides,nematicides, and molluscicides. Chemical classes of insecticides include2-dimethylaminopropane-1,3-dithiol, 2-dimethylaminopropane-1,3-dithiolanalogs, amidines, arylpyrroles, avermectin, benzoylureas, carbamates,carbamoyl-triazoles, cyclodienes, diacylhydrazines, dinitrophenols,fiprole, METI, neonicotinoids, non-ester pyrethroids, organochlorines,organophosphates, oxadiazines, oximes, carbamates, pyrethroids, andspinosyns. Suitable insecticides include1,1-bis(4-chlorophenyl)-2-ethoxyethanol, 1,1-dichloro-1-nitroethane,1,1-dichloro-2,2-bis(4-ethylphenyl)ethane, 1,2-dichloropropane with1,3-dichloropropene, 1-bromo-2-chloroethane,2-(1,3-dithiolan-2-yl)phenyl dimethylcarbamate, 2-(2-butoxyethoxy)ethylthiocyanate, 2-(4,5-dimethyl-1,3-dioxolan-2-yl)phenyl methylcarbamate,2-(4-chloro-3,5-xylyloxy)ethanol,2,2,2-trichloro-1-(3,4-dichlorophenyl)ethyl acetate, 2,2-dichlorovinyl2-ethylsulfinylethyl methyl phosphate, 2,4-dichlorophenylbenzenesulfonate, 2-chlorovinyl diethyl phosphate,2-isovalerylindan-1,3-dione, 2-methyl(prop-2-ynyl)aminophenylmethylcarbamate, 2-thiocyanatoethyl laurate, 3-bromo-1-chloroprop-1-ene,3-methyl-1-phenylpyrazol-5-yl dimethylcarbamate, 4-chlorophenyl phenylsulfone, 4-methyl(prop-2-ynyl)amino-3,5-xylyl methylcarbamate,4-methylnonan-5-ol with 4-methylnonan-5-one,5,5-dimethyl-3-oxocyclohex-1-enyl dimethylcarbamate,6-methylhept-2-en-4-ol, abamectin, acephate acequinocyl, acrinathrin,alanycarb, aldicarb, aldoxycarb, aldrin, allethrin [(1R)-isomers],allyxycarb, alpha-cypermethrin, amidithion, amidothioate, aminocarb,amiton; amiton hydrogen oxalate, amitraz, anabasine, aramite,athidathion, azadirachtin, azamethiphos, azinphos-ethyl,azinphos-methyl, azocyclotin, azothoate, barium polysulfide, Bayer22/190, Bayer 22408, bendiocarb, benfuracarb, bensultap, benzoximate,beta-cyfluthrin, beta-cypermethrin, bifenazate, bifenthrin, binapacryl,biopermethrin, bis(2-chloroethyl)ether, bistrifluoron, bromfenvinfos,bromocyclen, bromophos, bromophos-ethyl, bromopropylate, bufencarb,buprofezin, butacarb, butathiofos, butocarboxim, butonate,butoxycarboxim, cadusafos, calcium polysulfide, camphechlor,carbanolate, carbaryl, carbofuran, carbophenothion, carbosulfan, cartaphydrochloride, CGA 50 439, chinomethionat, chlorbenside, chlorbicyclen,chlordane, chlordecone, chlordimeform; chlordimeform hydrochloride,chlorethoxyfos, chlorfenapyr, chlorfenethol, chlorfenson,chlorfensulphide, chlorfluazuron, chlormephos, chloro-benzilate,chloromebuform, chloropropylate, chlorphoxim, chlorprazophos,chlorpyrifos, chlorpyrifos-methyl, chlorthiophos, chromafenozide,cloetho-carb, clofentezine, clothianidin, codlemone, coumaphos,coumithoate, crotoxyphos, crufomate, cryolite, CS 708, cyanofenphos,cyanophos, cyanthoate, cycloprothrin, cyfluthrin, cyhalothrin,cyhexatin, cypermethrin, cyphenothrin [(1R)-trans-isomers], cyromazine,DAEP, dazomet, DCPM, DDT, decarbofuran, deltamethrin, demephion;demephion-O; demephion-S, demeton; demeton-O; demeton-S,demeton-S-methyl, demeton-S-methylsulphon, diafenthiuron, dialifos,diazinon, dicapthon, dichlorvos, dicofol, dicrotophos, dicyclanil,dieldrin, dienochlor, diethyl 5-methyl-pyrazol-3-yl phosphate,diflubenzuron, dimefox, dimethoate, dimethrin, dimethylvinphos,dimetilan, dinex; dinex-diclexine, dinobuton, dinocap, dinocton,dinopenton, dinoprop, dinosulfon, dinotefuran, dinoterbon,dioxabenzofos, dioxacarb, dioxathion, diphenyl sulfone, disulfoton,dithicrofos, DNOC, dodec-8-enyl acetate, dofenapyn, DSP, EI 1642, emamectin benzoate, EMPC, empenthrin [(EZ)-(1R)-isomers], endosulfan,endothion, endrin, ENT 8184, EPBP, EPN, esfenvalerate, ethio-fencarb,ethion, ethiprole, ethoate-methyl, ethoprophos, etofenprox, etoxazole,etrimfos, famphur, fenazaflor, fenazaquin, fenbutatin oxide,fenchlorphos, fenethacarb, fenfluthrin, fenitrothion, fenobucarb,fenothio-carb, fenoxacrim, fenoxycarb, fenpirithrin, fenpropathrin,fenpyroximate, fenson, fensulfothion, fenthion, fentrifanil,fenvalerate, fipronil, flonicamid, fluacrypyrim, flubenzimine,flucofuron, flucycloxuron, flucythrinate, fluenetil, flufenoxuron,flufenprox, flumethrin, fluorbenside, fluvalinate, FMC 1137, fonofos,formetanate, formothion, formparanate, fosmethilan, fospirate,fosthiazate, fosthietan, furathiocarb, furethrin, gamma-cyhalo-thrin,gamma-HCH, glyodin, GY-81, halfenprox, halofenozide, heptachlor,heptenophos, hexadecyl cyclopropanecarboxylate, hexaflumuron,hexythiazox, hydramethylnon, hydroprene, hyquincarb, imidacloprid,imiprothrin, indoxacarb, iprobenfos, IPSP, isazofos, isobenzan, isodrin,isofenphos, isolane, isoprocarb, isopropylO-(methoxyaminothio-phosphoryl)salicylate, isothioate, isoxathion,jodfenphos, kelevan, kinoprene, lambda-cyhalothrin, leptophos, lirimfos,lufenuron, lythidathion, m-cumenyl methylcarbamate, malathion,malonoben, mazidox, MB-599, mecarbam, mecarphon, menazon, mephosfolan,mercurous chloride, mesulfenfos, metam, methacrifos, methamidophos,methanesulfonyl fluoride, methidathion, methiocarb, methocrotophos,methomyl, methoprene, methoquin-butyl, methothrin, methoxychlor,methoxyfenozide, methyl isothiocyanate, metolcarb, metoxadiazone,mevinphos, mexacarbate, milbemectin, mipafox, mirex, MNFA,monocrotophos, morphothion, naled, naphthalene, nicotine, nifluridide,nitenpyram, nithiazine, nitrilacarb; nitrilacarb 1:1 zinc chloridecomplex, nornicotine, novaluron, noviflumuron, O,O,O′O′-tetrapropyldithiopyrophosphate, O,O-diethyl O-4-methyl-2-oxo-2H-chromen-7-ylphosphorothioate, O,O-diethyl O-6-methyl-2-propylpyrimidin-4-ylphosphorothioate, O-2,5-dichloro-4-iodophenyl O-ethylethylphosphonothioate, oleic acid (fatty acids), omethoate, oxabetrinil,oxamyl, oxydemeton-methyl, oxydeprofos, oxydisulfoton, parathion,parathion-methyl, pentachlorophenol, permethrin, petroleum oils,phenkapton, phenothrin [(1R)-trans-isomer], phenthoate, phorate,phosalone, phosfolan, phosmet, phosnichlor, phosphamidon, phosphine,phoxim, phoxim-methyl, piperonyl butoxide, pirimetaphos, pirimicarb,pirimiphos-ethyl, pirimiphos-methyl, polychlorodicyclopentadieneisomers, polynactins, prallethrin, primidophos, proclonol, profenofos,promacyl, promecarb, propaphos, propargite, propetamphos, propoxur,prothidathion, prothiofos, prothoate, pymetrozine, pyraclofos,pyresmethrin, pyrethrins (pyrethrum), pyridaben, pyridalyl,pyridaphenthion, pyrimidifen, pyrimitate, pyriproxyfen, quinalphos,quinalphos-methyl, quinothion, quintiofos, R-1492, RA-17, resmethrin,rotenone, RU-15525, RU 25475, S421, sabadilla, schradan, silafluofen, SN72129, sodium fluoride, sodium hexafluorosilicate, sodium selenate,sophamide, spinosad, spirodiclofen, spiromesifen, spirotetramat(BYI8330), SSI-121, sulcofuron-sodium, sulfluramid, sulfosulfuron,sulfotep, sulfur, sulprofos, SZI-121, taroils, tazimcarb, TDE,tebufenozide, tebufenpyrad, tebupirimfos, teflubenzuron, tefluthrin,temephos, TEPP, terallethrin, terbufos, tetrachlorvinphos, tetradifon,tetramethrin, tetramethrin [(1R)-isomers], tetrasul, theta-cypermethrin,thiacloprid, thiamethoxam, thicrofos, thiocarboxime, thiocyclam,thiodicarb, thiofanox, thiometon, thionazin, thioquinox,thiosultap-sodium, tolfenpyrad, tralomethrin, transfluthrin,transpermethrin, triamiphos, triarathene, triazamate, triazophos,trichlorfon, trichloronat, trifenofos, triflumuron, trimedlure,trimethacarb, vamidothion, XMC, xylylcarb, zeta-cypermethrin,zolaprofos, and ZXI 8901.

Pigments and Dyes

Suitable colorants include pigments and dyes known in the art. Bothnatural and synthetic inorganic pigments can be used formulationsdescribed herein. Suitable natural inorganic pigments include naturaloxides, hydroxides, sulfides, sulfates, silicates, and carbonates ofmany mineral elements (e.g., iron, magnesium, potassium, aluminum, andcopper) as well as mixtures thereof. Red earths, yellow earths, greenearths, lapis lazuli, azurite, malachite, other traditional earthcolors, and mixtures thereof have been the main sources of naturalinorganic pigments. Suitable synthetic inorganic pigments include ferricammonium ferrocyanide, iron oxide, iron oxide yellow, iron oxide brown,iron oxide orange, iron oxide red, iron oxide black, iron blue, cobaltgreen, cobalt blue, zinc oxide, zinc sulfide, chrome titanium oxide(Pigment White 6), chromium oxide green (anhydrous), hydrated chromeoxide green, Prussian green, cyanine blue, manganese blue, manganeseviolet, titanium dioxide, and mixtures thereof. Furthermore, syntheticinorganic pigments made of oxide-coated micas, which may be eithertitanium dioxide or iron oxide coated micas, can also be used in thisinvention. Organic pigments in this invention include (using ColourIndex names) Pigment Blue 1, Pigment Blue 15, Pigment Blue 15:1, PigmentBlue 15:3, Pigment Blue 15:4, Pigment Blue 61, Pigment Blue 62, PigmentGreen 7, Pigment Green 36, Pigment Orange 5, Pigment Orange 13, PigmentOrange 16, Pigment Orange 34, Pigment Orange 36, Pigment Orange 46,Pigment Red 2, Pigment Red 3, Pigment Red 4, Pigment Red 12, Pigment Red17, Pigment Red 22, Pigment Red 23, Pigment Red 38, Pigment Red 48:1,Pigment Red 48:2, Pigment Red 48:3, Pigment Red 48:4, Pigment Red 49:1,Pigment Red 49:2, Pigment Red 52:1, Pigment Red 53:1, Pigment Red 57,Pigment Red 57:1, Pigment Red 60:1, Pigment Red 63:1, Pigment Red 81,Pigment Red 81:3, Pigment Red 90, Pigment Red 112, Pigment Red 169,Pigment Red 170, Pigment Red 202, Pigment Red 210, Pigment Violet 1,Pigment Violet 3, Pigment Violet 19, Pigment Violet 23, Pigment Violet27, Pigment Violet 29, Pigment Yellow 1, Pigment Yellow 3, PigmentYellow 12, Pigment Yellow 13, Pigment Yellow 14, Pigment Yellow 17,Pigment Yellow 62, Pigment Yellow 65, Pigment Yellow 73, Pigment Yellow74, Pigment Yellow 75, Pigment Yellow 83, Pigment Yellow 111, PigmentYellow 126, Pigment Yellow 168, Pigment Yellow 184, and mixturesthereof. The inorganic and organic pigment can be a dry powder, slurry,or suspension and can be high solids pigments. The solids content of thepigments can range from about 20 to 70%, the optimum range being from 30to 65%. Either the solids or the slurry can be post-added and stirred ineasily with agitation after the SC or SE formulation is made. The amountof the pigment in the formulation is from about 0.1 to 6%, preferablyfrom 0.1 to 2%.

Water-soluble dyes can be used in the formulations without stabilityproblems. Suitable dyes include Acid Black 172, Acid Black 194, AcidBlack 210, Acid Blue 1, Acid Blue 7, Acid Blue 9, Acid Blue 93, AcidBlue 93:1, Acid Green 16, Acid Green 25, Acid Orange 10, Acid Red 14,Acid Red 17, Acid Red 18, Acid Red 52, Acid Violet 17, Acid Violet 49,Acid Yellow 23, Acid Yellow 36, Basic Blue 26, Basic Blue 3, Basic Blue41, Basic Blue 54, Basic Blue 7, Basic Blue 9, Basic Brown 4, BasicBrown 1, Basic Green 1, Basic Green 4, Basic Orange 1, Basic Orange 2,Basic Orange 21, Basic Red 14, Basic Red 15, Basic Red 18, Basic Red 22,Basic Red 46, Basic Red 49, Basic Violet 1, Basic Violet 10, BasicViolet 14, Basic Violet 16, Basic Violet 2, Basic Violet 3, Basic Violet4, Basic Yellow 11, Basic Yellow 13, Basic Yellow 2, Basic Yellow 21,Basic Yellow 28, Basic Yellow, 9, Basic Yellow 37, Basic Yellow 40, D&CGreen 5, D&C Green 6, D&C Green 8, D&C Orange 4, D&C Orange 5, D&C Red17, D&C Red 21, D&C Red 22, D&C Red 27, D&C Red 28, D&C Red 30, D&C Red33, D&C Red 34, D&C Red 36, D&C Red 6, D&C Red 7, D&C Red 8, D&C Violet2, D&C Yellow 10, D&C Yellow 11, D&C Yellow 7, D&C Yellow 8, FD&C Blue1, FD&C Blue 2, FD&C Green 3, FD&C Red 3, FD&C Red 4, FD&C Red 40, FD&CYellow 5 (tartrazine), FD&C Yellow 6, and mixtures thereof. The dyes canbe post-added and stirred in easily with agitation after the SC or SEformulation is made. The amount of the dye in the formulation is fromabout 0.01 to 5%, the optimum range being from 0.02 to 2%.

Emulsifiers/Surfactants

Surfactants can be of the emulsifying or wetting type and can be ionicor nonionic. Representative surfactants include alkali metal, alkalineearth metal and ammonium salts of alkylsulfonic, phenylsulfonic ornaphthalenesulfonic acids; polycondensates of ethylene oxide with fattyalcohols or fatty acids or fatty amines or substituted phenols(particularly alkylphenols or arylphenols); ester-salts of sulfosuccinicacids; taurine derivatives, such as alkyl taurates; phosphoric esters;or esters of alcohols or polyoxyethylated phenols.

If a surfactant is used, it is preferential to use a nonionicsurfactant. However, the nonionic surfactant is used in an effectiveamount to improve the composition but in an amount to minimize foamingof the composition upon physical mixing or dilution into water.

Generally the amount of any nonionic surfactant is from 0.1 to 1% of thecomposition, preferably from 0.1 to 0.5% by weight of the composition.

A general description of surfactants that might be used include nonionicsurfactants such as C₈ to C₁₈ alcohol alkoxylates, both linear andbranched chain ethoxylates with 2 to 22 (preferably 2 to 10) ethyleneoxide (EO) units; alkyl phenol ethoxylates, mono- and di-nonyl and octylphenol with 2 to 150 (preferably 2 to 40) EO units, fatty aminealkoxylates, e.g., tallow, oleyl, stearyl and cocoamine alkoxylates with2 to 50 EO (preferably 2 to 20) units; alkanolamides; triglyceridealkoxylates, such as castor, rapeseed, soybean and colza oil ethoxylateswith 5 to 54 (preferably 5 to 20) EO units; sorbitan ester ethoxylateswith 20 to 30 EO units, ethylene oxide/propylene oxide copolymersincluding alkoxylated rapeseed oil with ethylene oxide and propyleneoxide chains; alkyl polyglycosides; fatty acid ethoxylates; fatty acidpolyethylene glycols; fatty alcohol ethoxylates; di- and tristyrylphenolethoxylates; glycerol esters; and polyol ethoxylate esters.

Polysorbates are a class of emulsifiers that can be used in thecompositions described herein. Polysorbates are oily liquids derivedfrom PEG-ylated sorbitan (a derivative of sorbitol) esterified withfatty acids. Surfactants that are esters of plain (non-PEG-ylated)sorbitan with fatty acids are usually referred to by the name Span.

Examples include, but are not limited to:

Polysorbate 20 (Tween 20 or polyoxyethylene (20) sorbitan monolaurate)

Polysorbate 40 (Tween 40 or polyoxyethylene (20) sorbitan monopalmitate)

Polysorbate 60 (Tween 60 or polyoxyethylene (20) sorbitan monostearate)

Polysorbate 80 (Tween 80 or polyoxyethylene (20) sorbitan monooleate)

The number 20 following the polyoxyethylene part refers to the totalnumber of oxyethylene —(CH₂CH₂O)— groups found in the molecule. Thenumber following the polysorbate part is related to the type of fattyacid associated with the polyoxyethylene sorbitan part of the molecule.Monolaurate is indicated by 20, monopalmitate is indicated by 40,monostearate by 60 and monooleate by 80. The same numbering is followedin their Span equivalents (Span 20, Span 40, Span 60 and Span 80).

Representative anionic surfactants include sulfates, fatty alcohol ethersulfates, fatty acid sulfates; sulfonates, alkylbenzenesulfonates, alkylnaphthalene sulfonates, alkylaryl sulfonates, olefin sulfonates,alkylphenol ethoxylate sulfates; phosphates, such as phosphates of fattyalcohol ethoxylate, phosphates of alkylphenol ethoxylate having 4 to 12EO units; alkyl sulfosuccinates; carboxylates, alkylphenol ethoxylatecarboxylates.

The compositions in accordance with the present invention may beformulated in any suitable manner appropriate to the ingredientsinvolved. Representative formulations are described below.

II. Formulations Including the Active Agents Described Herein

As described in more detail below, the formulations including the activeagents described herein can be in various liquid or solid forms, eitherfor application to a human or other animal, or to an article or locus.The various formulation types are described in detail below.

Formulations for Application to Animals or Humans

The composition can be formulated as a lotion composition foradministration to the skin of user. Such compositions may also contain,as inert ingredients, purified water, coconut oil, glycerin, geraniumoil, citric acid, lecithin, sodium bicarbonate and vanilla.

The compositions can also be formulated as spray compositions, forexample, for administration to the skin or fur of pets. Suchcompositions may contain 2% by weight of soy methyl ester, purifiedwater, coconut oil, glycerin, geranium oil, castor oil, lecithin andvanilla.

In one embodiment of the invention, the composition is formulated as aspray composition for administration to the skin of a user. Suchcomposition may contain from 0.1 to 15% by weight of the active agents,in a carrier base including, as inert ingredients, purified water,coconut oil, glycerin, geranium oil, citric acid, lecithin, sodiumbicarbonate and vanilla.

Other compositions of the invention may be formulated as sunblockcompositions, containing, in addition to soy methyl ester, zinc oxide,titanium dioxide, and/or small amounts of other sunscreen agents, aswell as ingredients such as coconut oil, purified water, glycerin,geranium oil, citric acid, lecithin, sodium bicarbonate, and vanilla.

Useful formulations for applying the compositions to an animal or ahuman, to combat pests such as mosquitoes, ticks, and the like, areadvantageously formulated as an emulsified base to which are addedcarrier, adjuvant and other ingredients of the composition.

Formulations for Application to a Locus

In addition to compositions of the invention that are formulated forapplication to body surfaces of users, compositions may be formulatedfor application or administration to any locus in which it is desired torepel pests against which the compositions of the invention arerepellently effective. Such loci may contain or include apparel,furniture, personal accessories, plastic products, cloth products,camping equipment, automotive and vehicular interiors, and the like. Forindoor or outdoor usage, the compositions of the invention may beformulated for broadcasting by misting systems or other distributionequipment.

Formulations for Spray and Aerosol Applications

Aerosol formulations typically include the active agents and a suitablepropellant (for example, n-butane). Alternatively, the active agents canbe dissolved or dispersed in a suitable medium, such as water or awater-miscible liquid, such as n-propanol, to provide compositions foruse in non-pressurized, hand-actuated spray pumps.

Ideally, the aerosol formulations provide a quick kill and rapidknock-down to flying insects. While not wishing to be bound to aparticular theory, it is believed that the presence of fatty acidsprovides both a rapid knock-down and quick kill to flying insects suchas bees, wasps, hornets, mosquitoes, flies, and the like.

In any of these forms, the formulations can include a propellant, sothat they can be aerosolized. Such aerosolized compositions can be usedin fumigation applications, such as ship/air cargo or food containmentareas. The compositions can also be used as a pesticide treatment priorto transporting items. In one embodiment, the compositions are convertedto aerosol compositions by adding nitrogen to the formula, and keepingthe contents in a pressurized container, such as a metal can. Nitrogenis an inert additive, and not a green-house gas, and can be preferredover other propellants, such as low molecular weight hydrocarbons. Whenpresent, the nitrogen is present in an amount of up to 10 percent,though is typically in the range of about 0.5% by weight of thecomposition.

The aerosol compositions can also include a propellant other thannitrogen, such as n-propane, n-butane, iso-pentane, iso-butane,n-pentane or hydrofluorocarbons.

Dispersible Concentrates

Dispersible Concentrates (DC) may be prepared by dissolving the activecompounds in water or an organic solvent, such as silicon oil, vegetableoil, or soy methyl ester. These solutions may contain, in addition tosodium lauryl sulfate, an additional surface active agent (for exampleto improve water dilution or prevent crystallization in a spray tank).

Solid Compositions

While the compositions described herein are mainly exemplified by liquidformulations, they can also exist as solids, where the sodium laurylsulfate is in the form of a solid salt rather than being present insolution, and the fatty acids, when present (which typically are lowmelting solids) are either in solid form, or are adsorbed or absorbedinto a solid carrier material. The soy methyl ester and/or undecanone,when present, can also be adsorbed or absorbed into a solid carriermaterial.

Solid homogenous or heterogenous compositions containing one or moreactive compounds described herein, for example, dusts (also known asdusting powders, dustable powders, and soluble powders), with a contentof the active compounds described herein ranging up to 80%), wettablepowders or granules, (including water-soluble and water-dispersiblegranules), particularly those obtained by extrusion, compacting,impregnation of a granular carrier, or granulation starting from apowder (the content of the active compounds described herein, in thesewettable powders or granules, being between about 0.5 and about 80%),baits, pellets, briquettes or capsules, may be used.

The formulation type chosen in any instance will depend upon theparticular purpose envisaged and the physical, chemical and biologicalproperties of the active compounds described herein.

Dustable powders (DP) may be prepared by mixing the active componentsdescribed herein with one or more solid diluents (for example naturalclays, kaolin, pyrophyllite, bentonite, alumina, montmorillonite,kieselguhr, chalk, diatomaceous earths, calcium phosphates, calcium andmagnesium carbonates, sulfur, lime, flours, talc and other organic andinorganic solid carriers) and mechanically grinding the mixture to afine powder.

Soluble powders (SP) may be prepared by mixing the active componentsdescribed herein with one or more water-soluble inorganic salts (such assodium bicarbonate, sodium carbonate or magnesium sulfate) or one ormore water-soluble organic solids (such as a polysaccharide) and,optionally, one or more wetting agents, one or more dispersing agents ora mixture of said agents to improve water dispersibility/solubility. Themixture is then ground to a fine powder. Similar compositions may alsobe granulated to form water soluble granules (SG).

Wettable powders (WP) (or powder for spraying) may be prepared by mixingthe active compounds described herein with one or more solid diluents orcarriers, one or more wetting agents and, preferably, one or moredispersing agents and, optionally, one or more suspending agents tofacilitate the dispersion in liquids. The mixture is then ground to afine powder. Similar compositions may also be granulated to form waterdispersible granules (WG). Each of these may be dissolved or suspendedin water to give any desired concentration and the resulting solution orsuspension can be employed very advantageously in particular forapplication to plant foliage.

Wettable powers are usually prepared so that they contain from about 10to about 80% by weight of active ingredients, from about 20 to about 90%of a solid carrier, from about 0 to about 5% of a wetting agent, fromabout 3 to about 10% of a dispersing agent and, when necessary, fromabout 0 to about 80% of one or more stabilizers and/or other additives,such as penetrating agents, adhesives, anti-caking agents, colorants, orthe like.

Granules (GR) may be formed either by granulating the active compoundsdescribed herein and one or more powdered solid diluents or carriers, orfrom pre-formed blank granules by absorbing the active compoundsdescribed herein (or a solution thereof, in a suitable agent) in aporous granular material (such as pumice, attapulgite clays, fuller'searth, kieselguhr, diatomaceous earths or ground corn cobs) or byadsorbing the active compounds described herein (or a solution thereof,in a suitable agent) on to a hard core material (such as sands,silicates, mineral carbonates, sulfates or phosphates) and drying ifnecessary. Agents which are commonly used to aid absorption oradsorption include solvents (such as aliphatic and aromatic petroleumsolvents, alcohols, ethers, ketones and esters) and sticking agents(such as polyvinyl acetates, polyvinyl alcohols, dextrins, sugars andvegetable oils). One or more other additives may also be included ingranules (for example an emulsifying agent, wetting agent or dispersingagent).

“Water dispersible granules (WG)” (granules which are readilydispersible in water) have compositions which are substantially close tothat of the wettable powders. They may be prepared by granulation offormulations described for the wettable powders, either by a wet route(contacting finely divided active ingredient with the inert filler and alittle water, e.g. 1 to 20% by weight, or with an aqueous solution of adispersing agent or binder, followed by drying and screening), or by adry route (compacting followed by grinding and screening).

In some embodiments, the solid compositions can include lubricants.Representative lubricants include precipitated silica and fumed alumina.Fumed alumina is produced by the hydrolysis of aluminum trichloride in ahydrogen-oxygen flame. The combustions process creates aluminum oxidemolecules which condense to form primary particles which sinter togetherto form aggregates. These aggregates have a chain-like structure and anaverage diameter of 0.1 and 0.2 microns. Fumed alumina, likeprecipitated silica, has small particle size in the submicron range (forprimary particle size of 20 nm and aggregate size of 150 nm) down tonanometer particle size with B.E.T. surface area of 55 m²/g. It alsoprovides rheology control and lubrication for the suspensionconcentrate.

Clays may also be optionally used in the present composition. Such claysinclude kaolinite, dickite, and nacrite, with the general formula ofAl₂Si₂O₅(OH)₄; pyrophylite, talc, vermiculite, sauconite, saponte,nontronite, and montmorillonite with the general chemical formula(Ca,Na,H)(Al,Mg,Fe,Zn)₂(Si,Al)₄O₁₀(OH)₂.xH₂O; attapulgite with thegeneral chemical formula Mg₅Si₈O₂₀(HO)₂(OH₂)₄4H₂O; and illite with thegeneral formula (K,H)Al₂(Si,Al)₄O₁₀(OH)₂.xH₂O.

The rates and concentrations of the formulated compositions may varyaccording to the method of application or the nature of the compositionsor use thereof.

III. Types of Pests that can be Treated

The compositions can be used to combat and control infestations of avariety of pests.

Pest species include arthropod pests, agricultural, horticulture, andgarden pests, rodent pests and reptile and amphibian pests. Arthropodpests include aphids, ants, bed bugs, bees (e.g. carpenter bees),beetles, centipedes, caterpillars, chiggers, cockroaches, crickets,cutworms, earwigs, fleas, flies (e.g., house flies, black flies, whiteflies, deer flies, fruit flies, horse flies, horn flies, midges, stableflies, etc.), fire ants, gnats, grasshoppers, hookworms, Japanesebeetles, June bugs, lice, locust, mealworms, mealybugs, millipedes,mites, mosquitoes, moths, pillbugs, scorpions, silverfish, spiders,stinkbugs, termites, thrips, ticks, and wasps. Agriculture, horticultureand garden pests include aphids, beetles, caterpillars, cutworms,maggots, mealybugs, mites (e.g. spider mites), moths, stinkbugs, thrips,and white flies. Rodent pests include chipmunks, mice, rats, squirrelsand voles. Reptile and amphibian pests include lizards, snakes, andfrogs.

Specific pests that were evaluated included flying insects, includingflies and wasps, lice, mites, spiders, carpenter bees, chiggers, ticks,fleas, ants, including fire ants, aphids, beetles (potato and bean),flea beetles, Japanese beetles, silver fish, cockroaches, fleahoppers,thrips, squash bugs, slugs, leaf hoppers, harlequin bugs and milk weedbugs. Representative insects that can be repelled using the compositionsdescribed herein include caterpillars, maggots, moths, and grasshoppers.Rodents and deer were also repelled with some formulations.

Based on the data on these specific pests, it is believed that thecompositions will be effective against a broad spectrum of pests, suchas Lepidoptera, Diptera, Hemiptera, Thysanoptera, Orthoptera,Dictyoptera, Coleoptera, Siphonaptera, Hymenoptera and Isoptera and alsoother invertebrate pests, for example, acarine, nematode and molluscpests. Insects, acarines, nematodes and molluscs are hereinaftercollectively referred to as pests. The pests which may be combated andcontrolled include those pests associated with agriculture (which termincludes the growing of crops for food and fiber products), horticultureand animal husbandry, companion animals, forestry and the storage ofproducts of vegetable origin (such as fruit, grain and timber); thosepests associated with the damage of man-made structures and thetransmission of diseases of man and animals; and also nuisance pests(such as flies).

Examples of pest species which may be controlled include: Myzus persicae(aphid), Aphis gossypii (aphid), Aphis fabae (aphid), Lygus spp.(capsids), Dysdercus spp. (capsids), Nilaparvata lugens (planthopper),Nephotettixc incticeps (leafhopper), Nezara spp. (stinkbugs), Euschistusspp. (stinkbugs), Leptocorisa spp. (stinkbugs), Frankliniellaoccidentalis (thrip), Thrips spp. (thrips), Leptinotarsa decemlineata(Colorado potato beetle), Anthonomus grandis (boll weevil), Aonidiellaspp. (scale insects), Trialeurodes spp. (white flies), Bemisia tabaci(white fly), Ostrinia nubilalis, (European corn borer), Spodopteralittoralis (cotton leafworm), Heliothis virescens (tobacco budworm),Helicoverpa armigera (cotton bollworm), Helicoverpa zea (cottonbollworm), Sylepta derogata (cotton leaf roller), Pieris brassicae(white butterfly), Plutella xylostella (diamond back moth), Agrotis spp.(cutworms), Chilo suppressalis (rice stem borer), Locusta migratoria(locust), Chortiocetes terminifera (locust), Diabrotica spp.(rootworms), Panonychus ulmi (European red mite), Panonychus citri(citrus red mite), Tetranychus urticae (two-spotted spider mite),Tetranychus cinnabarinus (carmine spider mite), Phyllocoptruta oleivora(citrus rust mite), Polyphagotarsonemus latus (broad mite), Brevipalpusspp. (flat mites), Boophilus microplus (cattle tick), Dermacentorvariabilis (American dog tick), Ctenocephalides felis (cat flea),Liriomyza spp. (leafminer), Musca domestica (housefly), Aedes aegypti(mosquito), Anopheles spp. (mosquitoes), Culex spp. (mosquitoes),Lucillia spp. (blowflies), Blattella germanica (cockroach), Periplanetaamericana (cockroach), Blatta orientalis (cockroach), termites of theMastotermitidae (for example Mastotermes spp.), the Kalotermitidae (forexample Neoterines spp.), the Rhinotermitidae (for example Coptotermesformosanus, Reticulitermes flavipes, R. speratu, R. virginicus, R.hesperus, and R. santonensis) and the Termitidae (for exampleGlobitermes sulphureus), Solenopsis geminata (fire ant), Monomoriumnpharaonis (pharaoh's ant), Damalinia spp. and Linognathus spp. (bitingand sucking lice), Meloidogyne spp. (root knot nematodes), Globoderaspp. and Heterodera spp. (cyst nematodes), Pratylenchus spp. (lesionnematodes), Rhodopholus spp. (banana burrowing nematodes), Tylenchulusspp. (citrus nematodes), Haemonchus contortus (barber pole worm),Caenorhabditis elegans (vinegar eelworm), and Trichostrongylus spp.(gastro intestinal nematodes).

IV. Pesticidal Methods of Treatment

The compositions described herein can be used to treat pest infestationsin crop loci, storage areas, property, and the like, and to treatanimals and humans exposed to, or likely to be exposed to, one or morepests. Individual methods of treatment are described in more detailbelow. In some embodiments, the compositions are used in agriculturalapplications, and can be non-phytotoxic or nearly so. In oneparticularly preferred embodiment, the compositions are used as a fireant drench. Where pests contribute allergens, the compositions canoptionally include an enzyme to assist with controlling allergens.

Treatment of Cargo/Food Containers/Storage Areas

The compositions can be applied to cargo holds, food containers, andstorage areas, for example, by fumigation, to control pests. Some of theformulas described herein are capable of being organically certified,and, when the compositions are intended for application to foodcontainers, it is preferable that such compositions are applied.

In these embodiments, the compositions can help prevent the spread ofinsects, arthropods, and other pests from one location to another,whether from one country to another, in the case of internationalshipments, or from one geographic area to another within the samecountry, in the case of domestic shipments.

Treatment of Specific Loci, Including Crop Loci

The compositions can be used to protect field, forage, plantation,glasshouse, orchard or vineyard crops, of ornamentals, or of plantationor forest trees, for example: cereals (such as wheat or rice), cotton,vegetables (such as peppers), field crops (such as sugar beets, soybeansor oil seed rape), grassland or forage crops (such as maize or sorghum),orchards or groves (such as of stone or pit fruit or citrus), ornamentalplants, flowers or vegetables or shrubs under glass or in gardens orparks, or forest trees (both deciduous and evergreen) in forests,plantations or nurseries.

The compositions can also be used to protect timber (standing, felled,converted, stored or structural) from attack, for example, by sawfliesor beetles or termites.

The compositions can be used to protect stored products such as grains,fruits, nuts, spices or tobacco, whether whole, milled or compoundedinto products, from moth, beetle, mite or grain weevil attack. Alsoprotected are stored animal products such as skins, hair, wool orfeathers in natural or converted form (e.g. as carpets or textiles) frommoth or beetle attack as well as stored meat, fish or grains frombeetle, mite or fly attack. In these embodiments, thenaturally-occurring and safe nature of the active agents is particularlyrelevant.

The compositions can be applied to grasses, shrubs, vegetable gardens,and fruit trees, in some embodiments, without phytotoxicity or withminimal phytotoxicity. As used herein, minimal phytotoxicity means thatthe leaves may experience browning by appearance, but no killing ordegradation to the plant, nor prevention of plant growth.

The amounts in which the compositions are applied can be varied within asubstantial range. They are generally on the order of magnitude which isconventionally chosen for the application of “attract-and-killformulations.”

Suitable means of applying the compositions to growing crops include asfoliar sprays (for example as an in-furrow spray), fogs or foams.

Suitable means of applying the compositions to soil or roots includeliquid drenches, smokes or foams. When a pest is soil-borne, thecomposition is distributed evenly over the area to be treated (i.e, forexample broadcast or band treatment) in any convenient manner and isapplied at rates from about 10 g/ha to about 400 g/ha, preferably fromabout 50 g/ha to about 200 g/ha. Application may be made, if desired, tothe field or crop-growing area generally or in close proximity to theseed or plant to be protected from attack. The compositions can beapplied before planting, at planting, or after planting but ideallybefore sprouting has taken place, or after sprouting. When used as adrench, the formulations can be particularly effective against all antspecies, including as fire ants, carpenter ants, red imported fire ants,Argentine ants, odorous house ants, pavement ants, and moisture ants.

Suitable means of applying the compositions to crop seeds includeapplication as seed dressings, e.g. by liquid slurries.

The compositions described herein can be applied to plants or areasunder cultivation in the form of droplets, drop-like areas or thindefined layers by using conventional devices as they are known to thoseskilled in the art. Fruit-bearing trees or of vines can advantageouslybe treated by applying the compositions using dosing dispensers,pipettes or syringes, brushing devises, or surface nozzles to distributethe compositions over a substantial area.

Suitable means of applying the compositions to the environment ingeneral or to specific locations where pests may lurk, including storedproducts, timber, household goods, or domestic or industrial premises,include sprays, fogs, dusts, smokes, lacquers, or baits.

In this embodiment, the compositions are generally applied to the locusin which the pest infestation is to be controlled at an effective ratein the range of about 2 g to about 1 kg of the active compounds perhectare of locus treated. Under ideal conditions, depending on the pestto be controlled, a lower rate may offer adequate protection. On theother hand, adverse weather conditions, resistance of the pest or otherfactors may require that the active ingredient be used at higher rates.The optimum rate depends usually upon a number of factors, for example,the type of pest being controlled, the type or the growth stage of theinfested plant, the row spacing or also the method of application.Preferably an effective rate range of the active compound is from about10 g/ha to about 400 g/ha, more preferably from about 50 g/ha to about200 g/ha.

Animal Treatment

The compositions can be used to control arthropods or helminths whichare injurious to, or spread or act as vectors of diseases domesticanimals, for example those hereinbefore mentioned, and more especiallyin the control of ticks, mites, lice, fleas, midges, or biting, nuisanceor myiasis flies.

Suitable means of applying the compositions to animals infested by orexposed to infestation by arthropods or helminths, include topicalapplication, such as by using pour-on formulations, sprays, baths, dips,showers, jets, dusts, greases, shampoos, creams, wax smears or livestockself-treatment systems. The frequency of treatment of the animal,preferably the domestic animal to be treated by the compositions, isgenerally from about once per week to about once per year, preferablyfrom about once every two weeks to once every three months.

Addition of Enzyme to Aid in Allergen Control

In some embodiments, the compositions can include an enzyme to assistwith allergen control, for example, allergens contributed by pests.

Although allergens are not specifically considered a pest, examples ofallergens include pollen, pet dander, mite and roach feces, and thelike. The and other allergens produced by pests (i.e., “pest-producedallergens”) can be controlled by administering the compositionsdescribed herein with an enzyme that degrades the allergens.

One representative enzyme is Subtilisin [CAS 9014-01-1], although othersinclude the enzymes in Kleen Kill® and Bactozyme®. Proteases are aspecifically-preferred class of enzymes for metabolizing pest-producedallergens. The term “protease” as used herein collectively denotesenzymes having properties for decomposing proteins and peptides. Theenzymes available in the invention may be any one of acidic, neutral andbasic proteases known in the art, per se. For example, they may beserine proteases such as trypsin, cysteine proteases such as papain,calpain and cathepsin B and cathepsin L, aspartic acid proteases such aspepsin, renin and cathepsin D, and proteases such as metalloproteases.The types and concentrations of enzymes can be appropriately selected bythose of skill in the art, with the knowledge of the particular type ofallergen to be degraded.

In one embodiment, when the compositions include the enzymes, theyfurther include 2-undecanone or rue oil. This combination of activeagents (i.e., enzyme and undecanone or rue oil) additive increases thetoxicity to hard bodied arthropods.

The advantages and features of the invention are further illustratedwith reference to the following examples, which are not to be construedas in any way limiting the scope of the invention but rather asillustrative of embodiments of the invention in specific applicationsthereof.

Example 1 Representative Compositions Specific Formulations:

Note: Emulsifiers may vary and individual formulant concentrations mayvary to yield a finished product with the desired consistency.

Formulation V: Sodium Lauryl Sulfate in Soybean Oil+Fatty Acids Oil inWater Emulsion

Water 75.0%  Sodium Lauryl Sulfate 5.8% Vegetable Oil (Soybean Oil and8.0% coconut Oil used) Coconut Oil Fatty Acids (C810 8.0% by P&G) SoyLecithin or polysorbate 20   2% Sodium Bicarbonate 1.0% Benzoic Acid,Sodium Salt 0.2% Total: 100% 

Formulation V1: Sodium Lauryl Sulfate in Soybean Oil+Water (No FA)

Water 64.2%  Sodium Lauryl Sulfate  5.8% Soybean Oil  30% Total: 100%

Formulation V2: Sodium Lauryl Sulfate in Coconut Oil+Water (No FA)

Water 64.2%  Sodium Lauryl Sulfate  5.8% Coconut Oil Triglyceride  30%Total: 100%

Formulation W: Sodium Lauryl Sulfate in Silicone Oil+Fatty Acids Oil inWater Emulsion

Water  75% Sodium Lauryl Sulfate 5.8% Coconut Oil Fatty Acids 8.0% (C810by Proctor & Gamble) Cyclomethicone silicone oil 8.0% (DC 345 of DowCorning) Polysorbate 20 2.0% Sodium Bicarbonate 1.0% Benzoic Acid,Sodium Salt 0.2% Total: 100% 

Formulation W1: Sodium Lauryl Sulfate in Silicone Oil+Water (No FA)

Water 74.2%  Sodium Lauryl Sulfate 5.8% Cyclomethicone (DC 345 of  20%Dow Corning) Total: 100% 

Formulation X: Sodium Lauryl Sulfate in SME+Fatty Acids Oil in WaterEmulsion

Water 85.2%   Sodium Lauryl Sulfate 5.8%   Soybean Methyl Ester (SME) 6%Coconut Oil Fatty Acids 3% (C810 by Proctor & Gamble) Total: 100% 

Formulation X1: Sodium Lauryl Sulfate in SME Low Percentage+Water (NoFA)

Water 88.2% Sodium Lauryl Sulfate  5.8% Soybean Methyl Ester (SME)   6%Total:  100%

Formulation X2: Sodium Lauryl Sulfate in SME High Percentage+Water (NoFA)

Water 64.2% Sodium Lauryl Sulfate  5.8% Soybean Methyl Ester (SME)   30%Total:  100%Formulation Y: Sodium Lauryl Sulfate with Undecanone Least-PhytotoxicFormulation

Water 67%  Sodium Lauryl Sulfate 6% Coconut Oil Triglyceride 4%(Capric/Caprylic Triglyceride) Coconut Fatty Acid C810 2% (Proctor &Gamble) Soybean Oil 4% Soy Methyl Ester 4% Undecanone 4% Silicone Oil(DC 345) 4% Polysorbate 20 2% Sodium Bicarbonate 0.5%   Benzoic Acid0.4%   Fragrance (Lavender) 1% Fragrance (Lemongrass 0.6%   Oil)Fragrance (Menthol or 0.5%   Peppermint Oil) Total: 100% Formulation Z: Shampoo Insecticide with Sodium Lauryl Sulfate+FattyAcids

Water 40%  Sodium Lauryl Sulfate 8% Cocamide DEA 3% Cocamidopropylbetaine 4% Olefin Sulfonate 2% Coconut Oil Triglyceride 6%(Capric/Caprylic Triglyceride) Coconut Fatty Acid C810 6% (Proctor &Gamble) Soybean Oil 8% Soy Methyl Ester 8% Silicone Oil (DC 345) or 8%Polysorbate 20 Hydrogenated Castor Oil 2% or Soy Lecithin Lauric Acid 1%Citric Acid 1% Sodium Bicarbonate 0.5%   Benzoic Acid 0.4%   Fragrance(Lavender) 1% Fragrance (Lemongrass 0.6%   Oil or Citral) Fragrance(Menthol or 0.5%   Peppermint Oil) Total: 100% 

Example 2 Evaluation of the Knock Down and Time to Mortality

The time various compositions take to both knock down (KD) and kill (TM)various pests was determined. As a control, results were compared usingsodium lauryl sulfate by itself, and with the various fatty acids.

Insects that were evaluated included flying insects, including flies andwasps, ticks, fleas, ants, including fire ants, aphids, Japanesebeetles, silver fish, and cockroaches.

The tests were conducted for a maximum observation time of 30 minutes,after which time, the test, and all observations, was stopped.

The individual testing protocols for each type of pest are describedbelow:

Flying Insects

Protocol: Each formula was put in a 16 oz bottle with trigger sprayerand sprayed on a broad area where the insect was flying or resting. Theaverage weight per area of spray was calculated. Insects specificallytested by this method included common house flies, mosquitoes (AsianTiger species), beetles (Japanese beetle), and moths (speciesundetermined) while the duration in seconds was observed for Knock Down(KD). Duration from contact of product to mortality (MT) was observed inseconds or minutes over a 30 minute observation. Observation wasdiscontinued at 30 minutes. See results in table above. Application ratewas approximately 0.01 oz per square inch or otherwise specified in thetable above.

Ticks

Protocol: Ticks (Lone Star species) were individually sprayed whiletraveling on the ground. The average amount of material per area wascalculated. The amount of material to kill the Tick was determined.

Fleas

Protocol: A light colored cotton towel was dragged across the sand andlet rest in an area where sand fleas were prevalent. The area on thetowel where the sand fleas landed was sprayed with the material using atrigger sprayer. The amount of material to kill the fleas wasdetermined.

Ants

Protocol: Ants (undetermined species) were individually sprayed whiletraveling on an indoor kitchen countertop. The average amount ofmaterial per area was calculated. The amount of material to kill the Antwas determined.

Fire Ants

Protocol: Fire ants (Red Imported species) were directly sprayed whiletraveling on the ground. The average amount of material per area wascalculated. The amount of material to kill the Fire Ant was determined.

Ag Insects (Aphids)

Protocol: Areas of vegetation containing aphids were sprayed withmaterial using a trigger sprayer. The average amount of material perarea was calculated. The time to mortality was observed.

Japanese Beetles

Protocol: Areas of Crepe Myrtle trees were sprayed containing JapaneseBeetles with material using a trigger sprayer. The average amount ofmaterial per area was calculated. The time to mortality was observed.

Spiders

Protocol: Spiders (Wolf species) were directly sprayed while travelingon the ground. The average amount of material per area was calculated.The amount of material to kill the Spider was determined.

Termites

Protocol: Termites (undetermined species) on the underside of a woodpile were sprayed with a trigger sprayer of material. The average amountof material per area was calculated. The amount of material to kill theTermites was determined.

Wasps

Protocol: The area where a Wasp was in flight or resting was sprayedusing a trigger sprayer. The minimum amount to kill the wasp in flightor while landed was determined as indicated in the table.

Silver Fish

Protocol: Silver Fish (undetermined species) were individually sprayedwhile traveling on an outdoor area of concrete. The average amount ofmaterial per area was calculated. The amount of material to kill theSilver Fish was determined.

Cockroaches

Beer was poured on a concrete floor in a garage to attract cockroaches.The cockroach was individually sprayed while feeding on the beer. Theaverage amount of material used was calculated.

Note: Mite and lice testing has not been conducted. However, based onthe results of this example, the compositions and methods would apply tomites and lice, as well as other insects and arthropods not directlylisted.

Table 1 describes the Efficacy results and resulting claims comparingSLS to SLS and Fatty Acids of Capric and Caprylic (nearly 50/50 butencompass any mixture). Table 2 compares Knock Down and cidal activityof SLS formulations without FAs of capric and caprylic.

TABLE 1 EFFICACY RESULTS - comparison of SLS + FA (capric/caprylic)formulas to SLS Formula U Formula V Formula W Formula X Formula YFormula Z Formulation Sodium Sodium Sodium Sodium Sodium shampooDescription Lauryl Lauryl Lauryl Lauryl Lauryl Sulfate InsecticideSulfate in Sulfate in Sulfate in Sulfate in with with water SoybeanOil + Silicon oil + SME + undecanone Sodium dilution Fatty Fatty AcidsFatty Acids (least- Lauryl using SLS Acids oil in oil in water oil inwater phytotoxic Sulfate + CONTROL water emulsion emulsion formulation)Fatty Acids emulsion low amount of FA Specific Diluted SLS 5.8% SLS 5.8%SLS 5.8% SLS 5.8% SLS 8% Formulation 1 part See other See other Seeother See other See other Chemistry formulants formulants formulantsformulants in formulants Store in Specific in Specific in SpecificSpecific in Specific material Formulation Formulation FormulationFormulation Formulation (29% section section section section belowsection solution) below below below below with additional 4 parts waterfor 5.8% total SLS solution Claims Range of SLS + SLS + SLS + SLS +SME + SLS + Fatty 0.1 to 10 vegetable Silicone oil modified undecanoneis Acids is percent SLS Oil (DC 345) + fatty acid highly insecticidalfor KD and (soybean oil Fatty Acids (Soy repellent and with MT orCoconut is highly Methyl insecticidal excellent enhancement Oil) + Fattyinsecticidal Ester) + with excellent KD and MT to Acids is with Fatty KDand MT; following highly excellent Acids is particularly formulas.insecticidal KD and MT highly effective at with repellent killing waspsexcellent and quickly KD and MT insecticidal with excellent KD and MTKnock Down Small Fly Small Fly Small Fly Small Fly Small Fly Small Fly(KD) and KD < 1 sec KD = immed KD = immed KD = KD = immed LandedMortality Dropped to MT < 30 sec MT < 30 sec immed MT < 10 sec MT < 10sec (MT) ground and MT < 10 sec Efficacy started Results walking after acouple minutes. Would not fly during observed time. MT > 30 min LargeFly Large Fly Large Fly Large Fly Large Fly Large Fly KD < 1 sec KD < 5sec KD < 5 sec KD < 1 sec KD < 1 sec Landed MT > 30 min MT = 5 min MT =5 min MT < 1 min MT < 1 min MT < 20 sec Aphid Aphid Aphid Aphid AphidAphid MT > 10 sec MT = immed MT = immed MT = MT = immed MT = immed immedMosquito Mosquito Mosquito Mosquito Mosquito Mosquito KD < 1 sec KD =immed KD = immed KD = KD = immed KD = immed MT = 5 min MT = immed MT =immed immed MT = immed MT = immed MT = immed Moth Not tested Not testedMoth (1 ml) Moth (1 ml) Not tested MT > 30 min KD < 1 sec KD < 1 sec MT= 2 min MT = 2 min Fleas Fleas Fleas Fleas Fleas Fleas KD = 10 KD =immed KD = immed KD = immed KD = immed KD = immed seconds MT = immed MT= immed MT = immed MT = immed MT = immed MT = 1 minute Ticks (4 ml) Tick(2 ml) Not tested Tick (1 ml) Tick (1 ml) Tick (1 ml) MT > 30 min MT = 4min MT < 60 sec MT < 60 sec MT < 30 sec (repellent on (repellent(repellent on (repellent on human skin) on human human skin) animalskin) skin) Roaches (8 ml) Adult Roach Adult Roach Adult Adult RoachAdult Roach Nymph (4 ml) (4 ml) Roach (4 ml) (4 ml) MT > 30 min MT < 30sec MT < 30 sec (4 ml) MT < 30 sec MT < 30 sec Nymph Nymph MT < 30 secNymph Roach Nymph Roach (2 ml) Roach (2 ml) Nymph (2 ml) Roach (2 ml) MT< 5 sec MT < 5 sec Roach MT < 5 sec MT < 5 sec (2 ml) MT < 5 sec Ants (2ml) Ants (1 ml) Ants (1 ml) Ants (1 ml) Ants (1 ml) Not tested MT =immed MT = immed MT = immed MT = immed MT = immed FIRE ANTS FIRE ANTSFIRE ANTS FIRE FIRE ANTS Not tested Application Applicaton ApplicationANTS Application rate = 4 ml rate = 2 ml rate = 2 ml Application Rate =1 ml MT = No MT = 30 sec MT = 30 sec Rate = 1 ml MT = 20 sec effect MT =20 sec Spider (8 ml) Spider (4 ml) Not tested Spider Spider (4 ml)Spider(2 ml) MT = no MT < 2 min (4 ml) MT < 30 sec MT = 10 sec effect MT< 1 min Jap Beetle Jap Beetle Jap Beetle Jap Beetle Jap Beetle Nottested (8 ml) (4 ml) (4 ml) (4 ml) (4 ml) MT = no MT < 5 sec MT < 5 secMT < 5 sec MT < 5 sec effect Termite Termite Termite Termite Termite (1ml) Termite (1 ml) (1 ml) (1 ml) (1 ml) MT < 20 sec (1 ml) MT = 20 secMT < 20 sec MT < 20 sec MT < 20 sec MT < 20 sec Wasps Wasp (4 ml) Nottested Wasp (4 ml) Wasp (2 ml) Not tested (8 ml) KD < 5 sec KD < 1 secKD < 1 sec KD < 5 sec MT = 30 sec MT = 20 sec MT = 20 sec MT = no effectSilver Fish Silver Fish Not tested Silver Fish Not tested Not tested (2ml) (2 ml) (2 ml) MT = no MT < 3 sec MT < 3 sec effect Dilution FIREANTS FIRE ANTS FIRE ANTS FIRE FIRE ANTS Not Tested ComparisonApplication Application Application ANTS Application rate = 4 ml rate =2 ml rate = 2 ml Application Rate = 1 ml observed for MT = 30 sec MT =30 sec Rate = 1 ml MT = 20 sec 10 minutes MT = 20 sec 1% SLS MT = noeffect 5% SLS MT = no effect 10% SLS MT = no effect (note, it took 20 mlof aqueous 10% SLS mixture to kill the fire ant.)

Results

The results outlined in Table 1 are summarized below.

Effectiveness Against Small Flies

With respect to small flies, the data in Table 1 show that sodium laurylsulfate, by itself, was able to immediately knock down flies, but notkill them. When fatty acids were added, alone or in combination withvegetable oil, silicon oil, or soy methyl ester, the time to kill wentfrom greater than 30 minutes, to less than 30 seconds. Thus, thecombination of sodium lauryl sulfate and fatty acids provided instantknockdown and almost instant kill. The results did not varysignificantly between using vegetable oil, silicon oil, or soy methylester. With very low amounts of fatty acids, and the use of undecanone,the composition also provided an almost instant kill

Effectiveness Against Large Flies

With respect to large flies, the data in Table 1 show that sodium laurylsulfate, by itself, was able to immediately knock down flies, but notkill them. When fatty acids were added, alone or in combination withvegetable oil, silicon oil, or soy methyl ester, the time to kill wentfrom greater than 30 minutes, to five minutes when vegetable oil orsilicon oil were added, to less than one minute when soy methyl esterwas used. Thus, soy methyl ester functioned better than vegetable oil orsilicon oil in this regard, providing both instant knockdown and almostinstant kill

With very low amounts of fatty acids, and the use of undecanone, thecomposition also provided an almost instant kill (i.e., less than oneminute).

Effectiveness Against Aphids

With respect to aphids, the data in Table 1 show that sodium laurylsulfate, by itself, was able to almost immediately kill then (i.e.,greater than 10 seconds). When all of the other formulations weretested, they provided an instant kill

Effectiveness Against Mosquitoes

With respect to mosquitoes, the data in Table 1 show that sodium laurylsulfate, by itself, was able to immediately knock down mosquitoes, butto kill them, it took around five minutes. When all of the otherformulations were tested, they provided an instant kill. Thus, theaddition of fatty acids, regardless of the other ingredients, providedan instant kill.

Effectiveness Against Moths

With respect to moths, the data in Table 1 show that sodium laurylsulfate, by itself, was unable to kill the moths, even at thirty minutespast exposure. Two other formulations were tested, namely, those witheither soy methyl ester, or undecanone. Both showed the ability to killmoths within around two minutes of exposure.

Effectiveness Against Fleas

With respect to fleas, the data in Table 1 show that sodium laurylsulfate, by itself, showed the ability knock down fleas in around tenseconds, and take around one minute to kill them. In contrast, when allof the other formulations were tested, they provided an instantknockdown and instant kill.

Effectiveness Against Ticks

With respect to ticks, the data in Table 1 show that sodium laurylsulfate, by itself, was unable to kill them, even after thirty minutesof exposure. When fatty acids and soybean oil were added, thecomposition acted as a repellent, and also killed the ticks in aroundfour minutes. All of the other formulations were tested, except for theformulation including silicon oil. All provided both insect repellentproperties, and killed the ticks within one minute of exposure.

Effectiveness Against Roaches

With respect to roaches, the data in Table 1 show that sodium laurylsulfate, by itself, was unable to kill nymph, even after thirty minutesof exposure. All of the other formulations were tested, and killed theadult roach in less than thirty seconds, and the nymph in less than fiveseconds.

Effectiveness Against Ants

With respect to ants, the data in Table 1 show that all formulationstested, including sodium lauryl sulfate by itself, and all of the otherformulations except the shampoo including fatty acids, immediatelykilled the ants.

With respect to fire ants, sodium lauryl sulfate by itself did not havethe ability to kill the fire ants. However, the formulations thatincluded the fatty acids and either silicon oil or soybean oil killedthe fire ants within thirty seconds. The formulations that included thefatty acids and soy methyl ester, and that included a low amount offatty acids, in combination with undecanone, both killed the fire antswithin twenty seconds.

A dilution study was done using just sodium lauryl sulfate and water. Ittook around 20 ml of an aqueous 10% sodium lauryl sulfate solution tokill the fire ants. No other dilution (1% or 5%) had any effect.

Effectiveness Against Spiders

With respect to spiders, the data in Table 1 show that sodium laurylsulfate, by itself, was unable to kill them, even after thirty minutesof exposure. When fatty acids and soybean oil were added, thecomposition killed the spiders in less than two minutes. When fattyacids and soy methyl ester were added, the spiders were killed in lessthan one minute. When undecanone was added, the spiders were killed inless than thirty seconds. The shampoo formulation including sodiumlauryl sulfate and the fatty acids killed the spiders in around tenseconds.

Effectiveness Against Japanese Beetles

With respect to Japanese beetles, the data in Table 1 show that sodiumlauryl sulfate, by itself, was unable to kill them, even after thirtyminutes of exposure. All other formulations tested (all but the shampooformulation were tested) killed the Japanese beetles in less than fiveseconds.

Effectiveness Against Termites

With respect to termites, the data in Table 1 show that sodium laurylsulfate, by itself, was able to kill termites in around 20 seconds. Allof the other formulations were tested, and each killed the termites inunder twenty seconds.

Effectiveness Against Wasps

With respect to wasps, the data in Table 1 show that sodium laurylsulfate, by itself, was able to almost instantaneously knock them down(i.e., knockdown in less than five seconds), but unable to kill them,even after thirty minutes of exposure. When formulations including fattyacids and silicon oil, soy methyl ester, or undecanone were tested, thecompositions killed the wasps in around thirty, twenty, and twentyseconds, respectively.

Effectiveness Against Silver Fish

With respect to silver fish, the data in Table 1 show that sodium laurylsulfate, by itself, was unable to kill them, even after thirty minutesof exposure. When formulations including fatty acids and silicon oil orsoy methyl ester were tested, the compositions each killed the silverfish in less than three seconds.

To verify that the results were due to the combination of fatty acidsand sodium lauryl sulfate, and not solely due to the presence of siliconoil, soybean oil, or soy methyl ester, additional formulations weretested. These formulations included:

Formula V1—Sodium lauryl sulfate in a soybean oil in water emulsion

Formula V Formula VI—Sodium lauryl sulfate in a soybean oil in wateremulsion

Formula W1—Sodium lauryl sulfate in a silicon oil in water emulsion

Formula W Formula VI—Sodium lauryl sulfate in a silicon oil in wateremulsion

Formula X1—Sodium lauryl sulfate in a soy methyl ester oil in wateremulsion

Formula X—Sodium lauryl sulfate and fatty acids in a soy methyl esteroil in water emulsion.

Thus, in these formulations, the presence or absence of the fatty acidswas measured with the three solvents, silicon oil, soybean oil, and soymethyl ester, in the form of oil-in-water emulsions. The results areshown in Table 2 below.

TABLE 2 COMPARATIVE CONTROLS (SLS without Fatty Acids compared to SLSwith Fatty Acids) Formula V1 Formula V Formula W1 Formula W Formula X1Formula X Formulation Sodium Sodium Sodium Sodium Sodium SodiumDescription Lauryl Sulfate Lauryl Lauryl Sulfate Lauryl Lauryl SulfateLauryl in Soybean Sulfate in in Silicon oil Sulfate in in SME in Sulfatein Oil in water Soybean Oil + in water Silicon oil + water SME +emulsion Fatty emulsion Fatty Acids emulsion Fatty Acids Acids oil inoil in water oil in water water emulsion emulsion emulsion Specific SLS5.8% in SLS 5.8% SLS 5.8% in SLS 5.8% SLS 5.8% in SLS 5.8% Formulationformula V1 See other formula W1 See other formula X1 See other (Soybeanoil formulants specified in formulants specified in formulants version)and in Specific Formulation in Specific Formulation in Specific V2(Coconut Formulation section. Formulation section. Formulation OilVersion) section section section specified in below below belowFormulation section. Claims SLS + SLS + SLS + SLS + SLS + SME SLS +vegetable oil vegetable Silicone Oil is Silicone oil increases modified(Soy and Oil effective at (DC 345) + knock down fatty acid coconut(soybean oil knocking Fatty Acids in flying (Soy tested) is or Coconutdown flying is highly insects and Methyl effective at Oil) + Fattyinsects but not insecticidal kills small Ester) + knocking Acids is veryeffective with insects such Fatty down flying highly at killingexcellent as Ants and Acids is insects and insecticidal insects. KD andMT Aphids highly limited at with Repellency is quickly but repellentkilling and excellent limited. larger insects, and repelling KD and MTarachnids and insecticidal small insects. arthropods not with as quickas excellent formulas KD and MT including the FAs of capric andcaprylic. Highly repellent against Japanese beetles, mosquitoes, ticksand roaches. Knock Small Fly Small Fly Small Fly Small Fly Small FlySmall Fly Down (KD) KD = immed KD = immed KD = immed KD = immed KD =immed KD = and MT > 30 min MT < 30 sec MT > 30 min MT < 30 sec MT = 15min immed Mortality MT < 10 sec (MT) Not tested Large Fly Not testedLarge Fly Not tested Large Fly Efficacy KD < 5 sec KD < 5 sec KD < 1 secResults MT = 5 min MT = 5 min MT < 1 min Aphid Aphid Aphid Aphid AphidAphid MT > 5 sec MT = immed MT > 10 sec MT = immed MT > 5 sec MT = immedMosquito Mosquito Mosquito Mosquito Mosquito Mosquito KD = immed KD =immed KD = immed KD = immed KD = immed KD = MT = 10 min MT = immed MT >30 min MT = immed MT = 4 min immed MT = immed Not tested Not tested Nottested Not tested Not tested Moth (1 ml) KD < 1 sec MT = 2 min FleasFleas Fleas Fleas Fleas Fleas KD < 1 sec KD = immed KD < 1 sec KD =immed KD < 1 sec KD = immed MT = 10 sec MT = immed MT = 20 sec MT =immed MT = 5 sec MT = immed Tick (2 ml) Tick (2 ml) Not Tested Nottested Tick (2 ml) Tick (1 ml) MT > 30 min MT = 4 min MT > 10 min MT <60 sec (and (repellent repellent on on human human skin) skin) NymphRoach Adult Roach Nymph Roach Adult Roach Nymph Roach Adult (4 ml) (4ml) (4 ml) (4 ml) (4 ml) Roach MT > 30 min MT < 30 sec MT > 30 min MT <30 sec MT = 10 min (4 ml) Nymph Nymph MT < 30 sec Roach (2 ml) Roach (2ml) Nymph MT < 5 sec MT < 5 sec Roach (2 ml) MT < 5 sec Ants (2 ml) Ants(1 ml) Ants (4 ml) Ants (1 ml) Ants (2 ml) Ants (1 ml) MT > 10 sec MT =immed MT > 30 sec MT = immed MT > 5 sec MT = immed Fire Ants FIRE ANTSFire Ants FIRE ANTS Fire Ants FIRE (4 ml) Application (4 ml) Application(4 ml) ANTS MT > 30 min rate = 2 ml MT > 30 min rate = 2 ml MT = 10 minApplication MT = 30 sec MT = 30 sec Rate = 1 ml MT = 20 sec Spider (8ml) Spider (4 ml) Not tested Not tested Spider (8 ml) Spider MT > 30 minMT < 2 min MT = 20 min (4 ml) MT < 1 min Jap Beetle Jap Beetle JapBeetle Jap Beetle Jap Beetle Jap Beetle (4 ml) (4 ml) (4 ml) (4 ml) (4ml) (4 ml) MT > 30 min MT < 5 sec MT > 30 min MT < 5 sec MT = 45 sec MT< 5 sec (observed repellency) Not tested Termite Not tested Termite Nottested Termite (1 ml) (1 ml) (1 ml) MT < 20 sec MT < 20 sec MT < 20 secWasp (8 ml) Wasp (4 ml) Wasp (8 ml) Not tested Wasp (8 ml) Wasp (4 ml)KD < 5 sec KD < 5 sec No effect KD < 1 sec KD < 1 sec MT > 30 min MT =30 sec MT > 30 min MT = 20 sec Not tested Silver Fish Not tested Nottested Not tested Silver Fish (2 ml) (2 ml) MT < 3 sec MT < 3 sec

Results

The results outlined in Table 2 are summarized below.

Effectiveness Against Small Flies

With respect to small flies, the data in Table 2 show that a combinationof sodium lauryl sulfate and either soybean oil or silicon oil was ableto immediately knock down small flies, but not kill them, even at thirtyminutes post exposure. The combination of sodium lauryl sulfate and soymethyl ester was able to kill the flies, but it took fifteen minutes todo so. In contrast, when fatty acids were present, the time to mortalitywas under thirty seconds for the emulsions including soybean or siliconoil, and under ten seconds for the emulsions including soy methyl ester.

Effectiveness Against Large Flies

With respect to large flies, the compositions were not tested withoutfatty acids being present. The combination of sodium lauryl sulfate,fatty acids, and either silicon oil or soybean oil took approximatelyfive seconds to knock down the flies, and around five minutes to killthem. In contrast, the combination of sodium lauryl sulfate, fattyacids, and soy methyl ester was able to knock down the flies in lessthan one second, and kill them in under one minute.

Effectiveness Against Aphids

With respect to aphids, the data in Table 2 show that a combination ofsodium lauryl sulfate and either soybean oil or soy methyl ester wasable to kill the aphids in around five seconds, and sodium laurylsulfate and silicon oil was able to kill the aphids in around tenseconds. The combination of sodium lauryl sulfate, fatty acids, and anyof soybean oil, silicon oil, or soy methyl ester was able to immediatelykill the aphids.

Effectiveness Against Mosquitoes

With respect to mosquitoes, the data in Table 2 show that all of theformulations were able to instantly knock down the mosquitoes. Thecombination of sodium lauryl sulfate and soybean oil took ten minutes tokill the mosquitoes, the combination of sodium lauryl sulfate andsilicon oil was did not kill the mosquitoes at thirty minutes postexposure, and the combination of sodium lauryl sulfate and soy methylester killed the mosquitoes within four minutes. In contrast, when fattyacids were present, the mosquitoes were instantly killed, regardless ofwhether the formulations included soybean oil, silicon oil, or soymethyl ester.

Effectiveness Against Moths

With respect to moths, only one formulation was tested. Thisformulation, a combination of sodium lauryl sulfate, fatty acids, andsoy methyl ester, was able to immediately knock down the moths, and thetime to mortality was around two minutes.

Effectiveness Against Fleas

With respect to fleas, the data in Table 2 show that all of theformulations knocked down the fleas, either instantaneously, or in lessthan one second. It took the combination of sodium lauryl sulfate andsoybean oil around ten seconds to kill the fleas, the combination ofsodium lauryl sulfate and silicon oil around twenty seconds to kill thefleas, and the combination of sodium lauryl sulfate and soy methyl esteraround five seconds to kill the fleas. The combination of sodium laurylsulfate, fatty acids, and any of soybean oil, silicon oil, or soy methylester, instantaneously killed the fleas.

Effectiveness Against Ticks

With respect to ticks, only combinations of sodium lauryl sulfate andsoybean oil or soy methyl ester, with or without fatty acids, weretested. The data in Table 2 show that a combination of sodium laurylsulfate and soybean oil was not able to kill ticks, even at thirtyminutes exposure, and the combination of sodium lauryl sulfate and soymethyl ester took around ten minutes to kill the ticks. In contrast,when fatty acids were added, the combination with soybean oil took fourminutes to kill the ticks, and the combination with soy methyl estertook less than one minute to kill the ticks. Further, both of the latterformulations repelled ticks from human skin.

Effectiveness Against Roaches

With respect to roaches, the data in Table 2 show that when fatty acidswere not present, nymph roaches were not killed even at thirty minutesexposure to a combination of sodium lauryl sulfate and silicon oil orsoybean oil, and it took ten minutes to kill roaches exposed to acombination of sodium lauryl sulfate and soy methyl ester. In contrast,when fatty acids were present, the time to mortality was under thirtyseconds, regardless of whether the formulations included soybean oil,silicon oil, or soy methyl ester.

Effectiveness Against Ants

With respect to ants, the data in Table 2 show that a combination ofsodium lauryl sulfate and soybean oil, silicon oil, or soy methyl esterwas able to kill the ants in around ten, thirty, and five seconds,respectively. In contrast, when fatty acids were present, the ants wereinstantly killed, regardless of whether the formulations includedsoybean oil, silicon oil, or soy methyl ester.

With respect to fire ants, the data in Table 2 show that a combinationof sodium lauryl sulfate and either soybean oil or silicon oil wasunable to kill fire ants, even at thirty minutes post exposure. Thecombination of sodium lauryl sulfate and soy methyl ester was able tokill the fire ants, but took ten minutes to do so. In contrast, whenfatty acids were present, the time to mortality was around thirtyseconds for the emulsions including soybean oil or silicon oil, andunder twenty seconds for the emulsions including soy methyl ester.

Effectiveness Against Spiders

With respect to spiders, only formulations including soybean oil and soymethyl ester were tested. The data in Table 2 show that a combination ofsodium lauryl sulfate and soybean oil was unable to kill spiders, evenat thirty minutes post exposure. The combination of sodium laurylsulfate and soy methyl ester was able to kill the spiders, but it tooktwenty minutes to do so. In contrast, when fatty acids were present, thetime to mortality was under two minutes for the emulsions includingsoybean oil, and under one minute for the emulsions including soy methylester.

Effectiveness Against Japanese Beetles

With respect to Japanese beetles, the data in Table 2 show that acombination of sodium lauryl sulfate and either soybean oil or siliconoil was unable to kill them, even at thirty minutes post exposure. Thecombination of sodium lauryl sulfate and soy methyl ester was able tokill the Japanese beetles in around forty five seconds. In contrast,when fatty acids were present, all formulations killed the Japanesebeetles in less than five seconds.

Effectiveness Against Termites

With respect to termites, only formulations including fatty acids weretested. The data in Table 2 show that all formulations killed thetermites in less than twenty seconds.

Effectiveness Against Wasps

With respect to wasps, the data in Table 2 show that a combination ofsodium lauryl sulfate and either soybean oil or soy methyl ester wasable to immediately knock down the wasps. However, the combination ofsodium lauryl sulfate and silicon oil was not able to knock down thewasps. Accordingly, the formulation with sodium lauryl sulfate, siliconoil, and fatty acids was not evaluated.

The combination of sodium lauryl sulfate and either soybean oil or soymethyl ester was unable to kill the wasps, even at thirty minutesexposure. In contrast, when fatty acids were present, the emulsionincluding soybean oil killed the wasps in thirty seconds, and theemulsion including soy methyl ester killed the wasps in twenty seconds.

Effectiveness Against Silver Fish

Only two of the formulations were tested on silver fish, theformulations with sodium lauryl sulfate, fatty acids, and either soybeanoil or soy methyl ester. The data in Table 2 show that both of theseformulations killed the silver fish in less than three seconds.

CONCLUSIONS

The combination of sodium lauryl sulfate and vegetable oil (for example,coconut and soybean oils) is effective at knocking down flying insects,but limited in its ability to kill or repel small insects.

The combination of sodium lauryl sulfate, vegetable oil (for example,coconut and soybean oils) and C₆₋₁₂ fatty acids is highly insecticidal,with excellent knock down and time to mortality.

The combination of sodium lauryl sulfate and silicon oil is effective atknocking down flying insects, but not very effective at killing insects.Repellency is limited. In contrast, the combination of sodium laurylsulfate, silicon oil, and C₆₋₁₂ fatty acids is highly insecticidal, withexcellent knock down and time to mortality.

The combination of sodium lauryl sulfate and soy methyl ester is moreeffective at knocking down flying insects than the combination of sodiumlauryl sulfate and either soybean oil or silicon oil, and is able toquickly kill small insects such as ants and aphids. However, thecombination required significantly more time to kill larger insects,arachnids, and arthropods than a comparable formula that included capricand/or caprylic acid. When these fatty acids were present, thecomposition was highly repellent and insecticidal, with excellentknockdown and time to mortality.

Example 3 Animal/Cattle Test

During the summer on a cattle ranch in Fayetteville, Ark., Formula X wasapplied on show cattle prior to them going to the Arkansas State Fair.Even in the show barns, there were no flies on the cattle, even thoughthey were abundant in the barns and arena.

Again, the product was applied two weeks later to a number of herd usedin the health program. The veterinarian normally applies Pymectrin aspart of the health program. Formula X was applied to 25 head and theresults for a two week period, including two small rain showers, wereequal to or better than the veterinarian-applied Permectrin.

Example 4 Testing and Results for Repellant Properties and a Comparisonof Pesticidal Properties vs. RAID™

Repellent Properties:

It was observed (as shown in Table 1, above) that compositions includingsodium lauryl sulfate, fatty acids and soy methyl ester were highlyrepellent in addition to being highly insecticidal. The compositionsincluding sodium lauryl sulfate, soy methyl ester, and undecanone werealso highly repellent in addition to being highly insecticidal.

With respect to ticks, sodium lauryl sulfate was not observed to beparticularly repellent on its own. In contrast, when fatty acids wereadded, alone or in combination with soybean oil or soy methyl ester, thecompositions were repellent when applied to human skin. Similarly,compositions including sodium lauryl sulfate and undecanone wererepellent to ticks when the compositions were applied to human skin.

Pesticidal Comparison with RAID®

Active: Tetramethrin 0.35%, Permethrin 0.10%, dcis/trans Allethrin 0.10%

The pesticidal effectiveness of Raid® Flying Insect Killer Formula 6 (SCJohnson) was compared to Formula X. Raid had no effect when sprayed onJapanese Beetles. RAID knocked down small flying insects such as fliesand mosquitoes, but took longer than 5 minutes to kill these insects.

RAID was ineffective against Ticks, Wasps and Carpenter bees. Incontrast, 2 ml of Formula X killed Japanese beetles, flies, mosquitoes,ticks in less than 1 minute and 4 ml killed wasps and Carpenter beeswithin 5 minutes.

Example 5 Field Evaluation of the Efficacy of Two Formulations AgainstMoisture Ants

An evaluation of the efficacy of two of the formulations describedherein at controlling moisture ants was conducted in southern Ontario.

The purpose of this study was to assess, under field conditions, theefficacy of the following formulations, with and without an enzymeadded, to control moisture ants (Lasius pallitarsis). Moisture ants canbe found making small mounds of excavated soil in lawns and lanewayssimilar to the more familiar pavement ants.

Formulation

3% Sodium Lauryl Sulfate

1% Lauric Acid

2.5% Potassium Oleate

4% Glycerin

2% Glycerol Monostearate

87.5% Water

(Optionally including an enzyme)

The enzyme is the enzyme registered under Chemical Abstracts No. [CAS9014-01-1]. Also suitable for use is the enzyme mixture known as“Bacto-Zyme,” produced by International Enzymes, Inc. of Las Vegas,Nev., as well as the various protease enzymes described herein. Theenzyme was present in a concentration of about 2.0% to about 10% byweight of the composition.

Materials and Methods

Site

The study was conducted utilizing a grass lawn and unpaved laneway. Thestudy area bordered a large mixed deciduous/coniferous woodlot (e.g.maples, poplars, birch, tamarack, white cedar, and white pine arepredominant species) with secondary growth under the canopy in a ruralarea four km south of the southern city limit of Guelph, Ontario.Adjacent to the study area was a cattail marsh (>four hectares)approximately 30 meters from the center of the study area.

Ant Nests

Prior to the start of the test, ant nests were located at the studysite. Each nest was marked with a numbered stake and ants were collectedfrom each nest. Ants were frozen and subsequently identified. The testproceeded when 15 nests were located and colony activity was laterconfirmed. Nests were at least 2 m apart but were typically 3-6 m apart.

Experimental Design

The test consisted of one trial with 15 nests of the ant Lasiuspallitarsis, the moisture ant. The trial consisted of ten treated nests(five per product) and five non-treated control nests. Treatments wereassigned randomly. Treatments and nests were designated as:

-   -   T1=nests T1-1 through T1-5    -   T2=nests T2-1 through T2-5    -   T3=nests T3-1 through T3-5    -   First number=treatment    -   Last number=rep    -   Treatment 1=Control    -   Treatment 2=Formulation without added enzyme    -   Treatment 3=Formulation with added enzyme

Observations

The study took place from Aug. 26 to Sep. 3, 2009. Observations weremade one day prior to treatment, the day of treatment (before treatment)and one, two, three, and seven days post-treatment. Observations weremade once a day. Time of observations was dependent on weather. On hotsunny days, ant activity was very low or non-existent mid-day soobservations were made early evening, 1800-1900 h. On overcast coolerdays observations were made afternoons, 1200-1600 h to ensure presenceof ant activity which could be otherwise lower if evenings were cool.Presence or forecast of rain also influenced observation times.

An observation consisted of a 2-minute count per nest. The number ofants entering and leaving the nest was counted or estimated and at theend of the 2-minute count, activity was also rated on a scale of 0-5.The rating scale used was as follows:

-   -   0 ants=0    -   21-50 ants=3    -   1-5 ants=1    -   51-75 ants=4    -   6-20 ants=2    -   >76 ants=5

Temperature and general weather conditions (wind, cloud cover,precipitation) were monitored at each observation time. At theconclusion of the trials two treated nests (one per product) and onecontrol nest from each trial was excavated. The number of live ants wasrecorded.

Treatment

Treatments took place from 1900-2000 h on Aug. 27, 2009. Both productswere poured into graduated hand mister bottles. To record the volumeapplied, the volume was recorded before and after each treatment. Theamount applied was relative to the size of the nest. A treatment wasdetermined to be complete when the nest was saturated. The mean amountapplied to moisture ant nests was 44.5±7.4 ml.

Data Analysis

The mean number of ants observed at treated and non-treated nests wascompared using analysis of variance and a Duncan's Multiple Range Test.Differences in the mean ant activity rating were determinednon-parametrically using the Kruskal-Wallis analysis of variance and theMann-Witney-Wilcoxon comparison of means. Data were analysed separatelyfor each day of observation and pre-treatment and post-treatment dayscombined. The analyses were completed using Statistical Analysis Systemsversion 6.12 (SAS Institute Inc., Cary, N.C.).

Results

Pre-treatment counts demonstrated that all nests had similar levels ofactivity and were not statistically different. Where the formulation didnot include any added enzyme, it provided approximately 94% control ofmoisture ants throughout the post-treatment observation period. Wherethe formulation included the added enzyme, it provided approximately 98%control of moisture ants throughout the post-treatment observationperiod. There was no statistical difference in the performance of thetwo products. For both products, differences in ant activity betweentreated and non-treated nests were statistically differentpost-treatment (P<0.05).

The mean temperature during observations was 20.2° C. (range=16.0,24.0). There was a single rain event on the night of August 28/29.Before the rain event, the nests were covered with a metal hoop andplastic bag to keep the nests dry overnight. Bags were removed the nextmorning.

At the conclusion of the trial, three nests were dug up (one pertreatment) and live ants were counted. For the nest treated with theformulation without added enzyme, zero ants were found. For the nesttreated with the formulation, with added enzyme, 10 ants were found.Upon examination of the control nest, 108 ants were counted.

TABLE 1 Mean number^(1,2) (± one standard deviation) of ants observed infield tests conducted near Guelph, Ontario, 2009, before and aftertreatment with two HOMS products. Formulation Without Formulation WithDay Control Enzyme Enzyme −1  21.2 ± 6.2 a 16.0 ± 5.7 a  17.6 ± 5.4 a  016.4 ± 4.2 a 15.6 ± 3.0 a  19.0 ± 4.2 a  1 18.6 ± 5.2 a 0 b 0.4 ± 0.4 b2 20.2 ± 4.9 a 1.0 ± 0.6 b 0.4 ± 0.2 b 3 18.6 ± 2.6 a 1.2 ± 1.0 b 0.4 ±0.2 b 7 40.4 ± 8.4 a 3.6 ± 2.1 b 0.4 ± 0.2 b Days pre- 18.8 ± 3.6 a 15.8± 3.0 a  18.3 ± 3.2 a  treatment Days post- 24.5 ± 3.4 a 1.5 ± 0.6 b 0.4± 0.1 b treatment ¹Values followed by different letters in the same roware significantly different (P < 0.05). ²Number of repetitions equalledfive.

TABLE 2 Mean activity rating^(1,2) (± one standard deviation) of antsobserved in field tests conducted near Guelph, Ontario, 2009, before andafter treatment with two HOMS products. Formulation Without FormulationWith Day Control Enzyme Enzyme −1  2.4 ± 0.2 a 2.2 ± 0.2 a 2.4 ± 0.2 a 02.4 ± 0.2 a 2.2 ± 0.2 a 2.4 ± 0.2 a 1 2.4 ± 0.2 a 0 b 0.2 ± 0.2 b 2 2.4± 0.2 a 0.4 ± 0.2 b 0.4 ± 0.2 b 3 2.2 ± 0.2 a 0.4 ± 0.2 b 0.4 ± 0.2 b 73.2 ± 0.4 a 0.8 ± 0.4 b 0.4 ± 0.2 b Days pre- 2.4 ± 0.2 a 2.2 ± 0.1 a2.4 ± 0.2 a treatment Days post- 2.6 ± 0.2 a 0.4 ± 0.1 b 0.4 ± 0.1 btreatment ¹Values followed by different letters in the same row aresignificantly different (P < 0.05). ²Number of repetitions equalledfive.

CONCLUSIONS

The two formulations, one with an enzyme, and one without, providedexcellent control of moisture ants (Lasius pallitarsis) in a field testin southern Ontario, Canada. The formulation without added enzymeprovided approximately 94% control of moisture ants throughout thepost-treatment observation period. The formulation with added enzymeprovided approximately 98% control of moisture ants throughout thepost-treatment observation period. There was no statistical differencein the performance of the two products.

Example 5 Phytotoxicity Testing

The following formulation was tested for phytotoxicity.

Formulation

3% Sodium Lauryl Sulfate

1% Lauric Acid

2.5% Potassium Oleate

4% Glycerin

2% Glycerol Monostearate

87.5% Water

(Optionally including an enzyme)

The formulation was applied at a concentration of approximately 1 oz persquare foot by spray application on the following vegetation. There wasno observed degradation of the vegetation after spraying and for eachweek of observation over a 6 week period after spraying.

-   -   Dandelion    -   Ivy    -   Rye grass    -   Fescue grass    -   Flowers including roses, hyacinth, gladiolas, hydrangea, azalea,        rhododendron and other ornamentals    -   Tomato plants    -   Squash plants    -   Carrot plants    -   Bean plants    -   Okra plants    -   Corn plants    -   Cucumber plants    -   Gardenia bushes    -   Crepe myrtle tree    -   Peach tree

This composition, and other compositions which, according to theprotocol identified above are non-phytotoxic or substantiallynon-phytotoxic, can be safely administered, such as by sprayadministration, to vegetation, lawns and gardens.

While the invention has been described herein in reference to specificaspects, features and illustrative embodiments of the invention, it willbe appreciated that the utility of the invention is not thus limited,but rather extends to and encompasses numerous other variations,modifications and alternative embodiments, as will suggest themselves tothose of ordinary skill in the field of the present invention, based onthe disclosure herein. Correspondingly, the invention as hereinafterclaimed is intended to be broadly construed and interpreted, asincluding all such variations, modifications and alternativeembodiments, within its spirit and scope.

1-33. (canceled)
 34. An article or region, to which has been applied apest-combating composition in the form of an oil-in-water emulsion, awater-in-oil emulsion, a micelle formulation, or an aerosol formulation,comprising an effective, pest-combatting amount of sodium lauryl sulfateand one or more C₆₋₁₂ fatty acids.
 35. The article or region of claim34, selected from the group consisting of apparel, furniture, personalaccessories, plastic articles, cloth articles, camping equipment,automotive and vehicular interiors.
 36. The article or region of claim34, selected from the group consisting of indoor and outdoor locations.37. The article or region of claim 34, wherein the amount of sodiumlauryl sulfate in the pest-combatting composition is between about 0.1and about 10 percent by weight of the composition.
 38. A method ofcombating pests, at a locus containing or susceptible to the presence ofsame, said method comprising applying to at least a portion of saidlocus a pest combatting composition, in the form of an oil-in-wateremulsion, a water-in-oil emulsion, a micelle formulation, or an aerosolformulation, comprising an effective, pest-combatting amount of sodiumlauryl sulfate and one or more C₆₋₁₂ fatty acids.
 39. The method ofclaim 38, wherein said pests comprise a pest selected from the groupconsisting of flies, mosquitoes, wasps, ants, ticks, fleas, cockroaches,silver fish, thrips, gnats, chiggers, aphids, Japanese beetles, mites,beetles (potato and bean), flea beetles, fleahoppers, squash bugs,slugs, leaf hoppers, harlequin bugs, milk weed bugs, spiders, lice,rodents, and deer.
 40. The method of claim 38, wherein the pest is anant, and the composition is applied in the form of a drench.
 41. Amethod of killing and/or repelling pests on an article or region incontact with, or susceptible to the presence of same, said methodcomprising applying to at least a portion of the article or region apest combatting composition, in the form of an oil-in-water emulsion, awater-in-oil emulsion, a micelle formulation, or an aerosol formulation,comprising an effective, pest-combatting amount of sodium lauryl sulfateand one or more C₆₋₁₂ fatty acids.
 42. The method of claim 41, whereinsaid pests comprise a pest selected from the group consisting of flies,mosquitoes, wasps, ants, ticks, fleas, cockroaches, silver fish, thrips,gnats, chiggers, aphids, Japanese beetles, mites, beetles (potato andbean), flea beetles, fleahoppers, squash bugs, slugs, leaf hoppers,harlequin bugs, milk weed bugs, spiders, lice, rodents, and deer. 43.The article or region of claim 34, wherein the composition exhibitsminimal or no phytotoxicity when applied to shrubs, grasses, vegetablegardens, and fruit trees.
 44. The article or region of claim 34, furthercomprising an enzyme, wherein the enzyme is a protease or helps tocontrol allergens contributed by pests.
 45. The method of claim 38,wherein the composition further comprises an enzyme, wherein the enzymeis a protease or helps to control allergens contributed by pests. 46.The method of claim 41, wherein the enzyme is a protease or helps tocontrol allergens contributed by pests.
 47. The method of claim 41,wherein the amount of sodium lauryl sulfate in the pest-combattingcomposition is between about 0.1 and about 10 percent by weight of thecomposition.
 48. The method of claim 41, wherein the article or regioncomprises a textile.
 49. The method of claim 41, wherein the method isused in agricultural or horticultural applications.
 50. The article orregion of claim 34, wherein the composition further comprises soy methylester.
 51. The article or region of claim 34, wherein the compositionfurther comprises 2-undecanone or rue oil.
 52. The article or region ofclaim 34, wherein the composition further comprises a carrier oil, anessential oil, or a botanical extract.
 53. The article or region ofclaim 52, wherein the carrier oil is silicon oil or a vegetable oil. 54.The article or region of claim 52, wherein the essential oil is selectedfrom the group consisting of peppermint oil, menthol, citral, lemongrassoil, and cedar oil.
 55. The article or region of claim 34, wherein thefatty acids comprise one or more of lauric, capric or caprylic acid. 56.The article or region of claim 34, wherein the composition is in theform of a lotion, spray, crème, or aerosol.
 57. The article or region ofclaim 34, wherein the amount of sodium lauryl sulfate in the compositionis in the range of between about 1 and 10% by weight of the composition.58. The article or region of claim 34, wherein the composition furthercomprises at least one additional active or inactive ingredient.
 59. Thearticle or region of claim 58, wherein the at least one additionalactive or inactive ingredient comprises an ingredient selected from thegroup consisting of additional pest-combating ingredients.
 60. Thearticle or region of claim 58, wherein the composition comprises aningredient selected from the group consisting of pest repellents andcidal agents.
 61. The article or region of claim 34, wherein thecomposition further comprises a second insect repellent or cidalingredient.
 62. The article or region of claim 34, wherein thecomposition further comprises a sticking agent or a thixotropic agent.63. The article or region of claim 34, wherein the article or regioncomprises a textile.
 64. The article or region of claim 34, wherein thearticle or region is selected from the group consisting of apparel,furniture, personal accessories, plastic products, cloth products,camping equipment, and automotive and vehicular interiors.
 65. Thearticle or region of claim 34, wherein the article or region comprisesshrubs, grasses, vegetable gardens, or fruit trees.
 66. The article orregion of claim 34, wherein the article or region comprises livestock.67. A pest-combatting composition comprising sodium lauryl sulfate, athixotropic agent or thickening agent, and one or more C₆₋₁₂ fattyacids.
 68. The composition of claim 67, wherein the amount of sodiumlauryl sulfate is between about 0.1 and 10 percent by weight of thecomposition.
 69. The composition of claim 67, further comprising anenzyme that is a protease or that helps to control allergens contributedby pests.
 70. The composition of claim 69, wherein the protease is aserine protease, cysteine protease, aspartic acid protease, ormetalloprotease.
 71. The method of claim 41, wherein the pest-combattingcomposition further comprises an enzyme that helps to control allergenscontributed by pests, and wherein the method further controls allergensin the article or region to which the composition is applied.